Variant DetailsVariant: esv2657534![](http://dgv.tcag.ca/gb2/gbrowse_img/dgv2_hg38/?name=chr19:56086979..56089623;width=800;overview=1) Internal ID | 9576953 | Landmark | | Location Information | | Cytoband | 19q13.43 | Allele length | Assembly | Allele length | hg38 | 2645 | hg19 | 2648 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6362205, essv5537606, essv6419958, essv5887212, essv5643774, essv5991756, essv5970511, essv6361176, essv6554356, essv5792796, essv5693662, essv6071864, essv6278974, essv5612512, essv5516718, essv5628177, essv5396224, essv6208346, essv5928920, essv6435257, essv6376735, essv6108933, essv6328823, essv6494235, essv6488796, essv5434594, essv5635407, essv6427887, essv6115670, essv5412689, essv5615800, essv6385395, essv6155493, essv5978546, essv6479006, essv6570196, essv5564206, essv5601412, essv5410326, essv6190316, essv5699482, essv5490122, essv5826674, essv5548782, essv5843588, essv6498507, essv5900098, essv5738436, essv5842832, essv5758520, essv6243076, essv6001225, essv5472784, essv5743552, essv6430169, essv6179067, essv5995389, essv6258500, essv5755410, essv5889037, essv6087079, essv6566057, essv5916590, essv5594187, essv6142555, essv6140548, essv6266342, essv5977513, essv6206298, essv5984709, essv5540493, essv6378600, essv5626556, essv5474947, essv5432412, essv6190158, essv5946285, essv5487233, essv5496484, essv6295454, essv6306926, essv6447975, essv6222319, essv5442748, essv6247752, essv6544758 | Samples | HG00626, HG00650, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00524, HG00699, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00610, HG00537, HG00590, HG00512, HG00683, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00596, HG00557, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00635, HG00651, HG00690, HG00404, HG00531, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00656, HG00698, HG00595, HG00472, HG00628, HG00437, HG00581 | Known Genes | ZNF787 | 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) | esv2657534
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 86 | Observed Complex | 0 | Frequency | n/a |
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