Variant DetailsVariant: esv2667097Internal ID | 9586516 | Landmark | | Location Information | | Cytoband | 11p15.4 | Allele length | Assembly | Allele length | hg38 | 196 | hg19 | 196 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5493819, essv5618486, essv6407796, essv5908769, essv6420475, essv6470918, essv6237966, essv6007492, essv6179142, essv6366640, essv6347607, essv5771721, essv6218505 | Samples | NA18508, NA18498, NA18520, NA19663, NA18499, NA18853, NA19225, NA18909, NA20281, NA18501, NA19093, NA19102, NA18505 | Known Genes | APBB1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2667097
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
|
|