nsv4352369 - (obsolete)
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:
- Submitted on:GRCh37 (hg19)
- Variant Calls:0
- Validation:Not tested
- Clinical Assertions: No
- Region Size:33,491,909
- Description:GRCh38/hg38 21q11.2-22.3(chr21:7749532-46649831)x3 AND See cases
Source: NCBI
This variant has been obsoleted and is no longer valid.