Variant DetailsVariant: esv3610895 Internal ID | 6651120 | Landmark | | Location Information | | Cytoband | 6q23.3 | Allele length | Assembly | Allele length | hg38 | 1543 | hg19 | 1543 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12559759, essv12559764, essv12559747, essv12559757, essv12559751, essv12559753, essv12559750, essv12559768, essv12559760, essv12559766, essv12559769, essv12559758, essv12559761, essv12559748, essv12559770, essv12559754, essv12559755, essv12559763, essv12559749, essv12559765, essv12559756, essv12559767, essv12559752, essv12559762 | Samples | HG02944, HG00640, NA19092, HG01051, HG00641, HG01325, HG03099, HG01110, HG03209, HG01308, HG03267, NA19200, HG02943, HG01248, HG02878, NA18907, HG03301, HG01073, HG01958, HG01396, NA19467, HG03279, HG01055, HG01097 | Known Genes | AHI1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3610895
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
|
|