esv2422010
- Organism: Homo sapiens
- Study:estd195 (Altshuler et al. 2010)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:NCBI36 (hg18)
- Variant Calls:36
- Validation:Not tested
- Clinical Assertions: No
- Region Size:4,287
- Publication(s):International HapMap 3 Consortium et al. 2010
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 326 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 326 SVs from 46 studies. See in: genome view
Overlapping variant regions from other studies: 139 SVs from 15 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv2422010 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| esv2422010 | Remapped | Perfect | GRCh37.p13 | Primary Assembly | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| esv2422010 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000012.10 | Chr12 | 945,143 | 949,429 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Copy number | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv5004648 | deletion | NA19466 | SNP array | SNP genotyping analysis | 1 | 144 |
| essv5005929 | deletion | NA18516 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5011552 | deletion | NA19319 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5019465 | deletion | NA19118 | SNP array | SNP genotyping analysis | 1 | 127 |
| essv5024821 | deletion | NA21613 | SNP array | SNP genotyping analysis | 1 | 149 |
| essv5026082 | deletion | NA21408 | SNP array | SNP genotyping analysis | 1 | 131 |
| essv5027070 | deletion | NA21436 | SNP array | SNP genotyping analysis | 1 | 143 |
| essv5031092 | deletion | NA21425 | SNP array | SNP genotyping analysis | 1 | 128 |
| essv5032536 | deletion | NA21312 | SNP array | SNP genotyping analysis | 1 | 129 |
| essv5036891 | deletion | NA21617 | SNP array | SNP genotyping analysis | 1 | 155 |
| essv5041026 | deletion | NA21423 | SNP array | SNP genotyping analysis | 0 | 136 |
| essv5046692 | deletion | NA21313 | SNP array | SNP genotyping analysis | 1 | 140 |
| essv5050403 | deletion | NA21520 | SNP array | SNP genotyping analysis | 1 | 139 |
| essv5063240 | deletion | NA21479 | SNP array | SNP genotyping analysis | 1 | 144 |
| essv5072721 | deletion | NA21314 | SNP array | SNP genotyping analysis | 1 | 134 |
| essv5074344 | deletion | NA21580 | SNP array | SNP genotyping analysis | 1 | 136 |
| essv5088526 | deletion | NA19179 | SNP array | SNP genotyping analysis | 1 | 155 |
| essv5094195 | deletion | NA21526 | SNP array | SNP genotyping analysis | 1 | 144 |
| essv5100268 | deletion | NA19332 | SNP array | SNP genotyping analysis | 1 | 141 |
| essv5105041 | deletion | NA19818 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5106109 | deletion | NA19310 | SNP array | SNP genotyping analysis | 1 | 154 |
| essv5106197 | deletion | NA21480 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5107057 | deletion | NA21521 | SNP array | SNP genotyping analysis | 1 | 130 |
| essv5108703 | deletion | NA21368 | SNP array | SNP genotyping analysis | 1 | 137 |
| essv5114184 | deletion | NA21583 | SNP array | SNP genotyping analysis | 1 | 149 |
| essv5120972 | deletion | NA19098 | SNP array | SNP genotyping analysis | 1 | 132 |
| essv5124320 | deletion | NA21587 | SNP array | SNP genotyping analysis | 1 | 138 |
| essv5124842 | deletion | NA21527 | SNP array | SNP genotyping analysis | 0 | 133 |
| essv5125168 | deletion | NA21435 | SNP array | SNP genotyping analysis | 1 | 125 |
| essv5127585 | deletion | NA21405 | SNP array | SNP genotyping analysis | 1 | 139 |
| essv5130393 | deletion | NA21512 | SNP array | SNP genotyping analysis | 1 | 124 |
| essv5133473 | deletion | NA21634 | SNP array | SNP genotyping analysis | 1 | 128 |
| essv5138459 | deletion | NA21364 | SNP array | SNP genotyping analysis | 1 | 142 |
| essv5140572 | deletion | NA21599 | SNP array | SNP genotyping analysis | 1 | 133 |
| essv5154761 | deletion | NA21360 | SNP array | SNP genotyping analysis | 1 | 135 |
| essv5157905 | deletion | NA21473 | SNP array | SNP genotyping analysis | 1 | 163 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv5004648 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5005929 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5011552 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5019465 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5024821 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5026082 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5027070 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5031092 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5032536 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5036891 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5041026 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5046692 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5050403 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5063240 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5072721 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5074344 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5088526 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5094195 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5100268 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5105041 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5106109 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5106197 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5107057 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5108703 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5114184 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5120972 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5124320 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5124842 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5125168 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5127585 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5130393 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5133473 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5138459 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5140572 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5154761 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5157905 | Remapped | Perfect | NC_000012.12:g.(?_ 965716)_(970002_?) del | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 965,716 | 970,002 |
| essv5004648 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5005929 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5011552 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5019465 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5024821 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5026082 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5027070 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5031092 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5032536 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5036891 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5041026 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5046692 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5050403 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5063240 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5072721 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5074344 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5088526 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5094195 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5100268 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5105041 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5106109 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5106197 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5107057 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5108703 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5114184 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5120972 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5124320 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5124842 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5125168 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5127585 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5130393 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5133473 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5138459 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5140572 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5154761 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5157905 | Remapped | Perfect | NC_000012.11:g.(?_ 1074882)_(1079168_ ?)del | GRCh37.p13 | First Pass | NC_000012.11 | Chr12 | 1,074,882 | 1,079,168 |
| essv5004648 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5005929 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5011552 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5019465 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5024821 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5026082 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5027070 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5031092 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5032536 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5036891 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5041026 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5046692 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5050403 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5063240 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5072721 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5074344 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5088526 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5094195 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5100268 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5105041 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5106109 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5106197 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5107057 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5108703 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5114184 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5120972 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5124320 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 | ||
| essv5124842 | Submitted genomic | NC_000012.10:g.(?_ 945143)_(949429_?) del | NCBI36 (hg18) | NC_000012.10 | Chr12 | 945,143 | 949,429 |