Variant DetailsVariant: esv2659073Internal ID | 9578492 | Landmark | | Location Information | | Cytoband | 15q26.1 | Allele length | Assembly | Allele length | hg38 | 2314 | hg19 | 2314 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6315546, essv5903312 | Samples | HG00692, NA18628 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2659073
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
|
|