Variant DetailsVariant: esv2670643 Internal ID | 9590062 | Landmark | | Location Information | | Cytoband | 22q13.1 | Allele length | Assembly | Allele length | hg38 | 32748 | hg19 | 32748 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv833e199 | Supporting Variants | essv5709561, essv5622471, essv5728731, essv5622235, essv5397597, essv6251417, essv5845191, essv6533256, essv5905084, essv5911014, essv6201462, essv6544990, essv5793420, essv6521162, essv5833805, essv6231233, essv6060130, essv6584113, essv6072606, essv5502791, essv6392234, essv5459411, essv5931933, essv6043454, essv5536834, essv5490649, essv6415203, essv5940053, essv5823166, essv5944766, essv5886854, essv6467091, essv5411671, essv5531318, essv6495429, essv6320272, essv5541741, essv6547992, essv6173476, essv5553344, essv6283970, essv6294165, essv6544208, essv6499182, essv6165955, essv6179838, essv5889803, essv6231896, essv6110546, essv5849918, essv5467131, essv5672403 | Samples | HG00650, HG00542, HG00608, HG00671, HG00559, HG00699, HG00566, HG00589, HG00501, HG00634, HG00590, HG00512, HG00422, HG00427, HG00530, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00557, HG00428, HG00653, HG00701, HG00657, HG00556, HG00533, HG00500, HG00708, HG00635, HG00651, HG00690, HG00404, HG00531, HG00684, HG00525, HG00704, HG00625, HG00580, HG00473, HG00418, HG00707, HG00672, HG00614, HG00478, HG00421, HG00656, HG00698, HG00472, HG00437, HG00593 | Known Genes | APOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2670643
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 52 | Observed Complex | 0 | Frequency | n/a |
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