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| Status |
Public on Mar 28, 2020 |
| Title |
High copy number variation burdens in cranial meningiomas from patients with diverse clinical phenotypes characterized by hot genomic structure changes |
| Organism |
Homo sapiens |
| Experiment type |
SNP genotyping by SNP array
Genome variation profiling by SNP array
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| Summary |
Meningiomas, as the most common primary tumor of the central nervous system, are known to harbor genomic aberrations that associate with clinical phenotypes. Here we performed genome-wide genotyping for cranial meningiomas in 383 Chinese patients and identified 9,821 copy number variations (CNVs).
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| Overall design |
Genome-wide genotyping was performed for cranial meningiomas in 383 Chinese patients and identified 9,821 copy number variations (CNVs).
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| Contributor(s) |
Wang L, Zhang D, Wu Z |
| Citation missing |
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| |
| Submission date |
Mar 27, 2020 |
| Last update date |
Mar 30, 2020 |
| Contact name |
Dake Zhang |
| E-mail(s) |
zhangdk@big.ac.cn
|
| Organization name |
Beijing Institute of Genomics, Chinese Academy of Sciences
|
| Street address |
NO.1 Beichen West Road, Chaoyang District
|
| City |
Beijing |
| ZIP/Postal code |
100101 |
| Country |
China |
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| Platforms (1) |
| GPL28320 |
Illumina Human Infinium CoreExome-24 Genotyping BeadChip (HumanCoreExome-24 v1.0) |
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| Samples (383)
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| Relations |
| BioProject |
PRJNA615929 |
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