Variant DetailsVariant: esv2662850 Internal ID | 9582269 | Landmark | | Location Information | | Cytoband | 11q13.1 | Allele length | Assembly | Allele length | hg38 | 274 | hg19 | 274 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6294468, essv5926740, essv6590699, essv5966949, essv5775550, essv6384615, essv5770818, essv5984642, essv5431231, essv5413724, essv6526726, essv5691640, essv5865659, essv6060468, essv5548420, essv6045978, essv5702613, essv5397104, essv6199116, essv5656596, essv5947876, essv5584638, essv5859453, essv6385293 | Samples | NA18565, HG00654, NA18595, NA18560, HG00534, NA18557, NA18638, HG00464, HG00428, HG00653, HG00556, HG00583, NA18948, HG00531, NA18536, HG00476, HG00607, HG00707, HG00513, HG00698, NA18552, NA18624, NA18623, NA18612 | Known Genes | SNX32 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2662850
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
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