nsv4728394
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:1,535,739
- Description:GRCh37/hg19 2p22.2-22.1(chr2:38012532-39548268)x3 AND not provided