nsv6636352
- 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:231,151
- Description:GRCh37/hg19 2p22.1(chr2:39040762-39271911)x1 AND not provided