Variant DetailsVariant: esv2669581 | Internal ID | 9935686 | | Landmark | | | Location Information | | | Cytoband | 17q25.3 | | Allele length | | Assembly | Allele length | | hg38 | 2300 | | hg19 | 2300 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5778018, essv5554103, essv5751890, essv6196409, essv6092267, essv5430145, essv6592424, essv6210149, essv5770276, essv6442774, essv5533933, essv6010930, essv6403043, essv6058633, essv5460660, essv6588793, essv5839441, essv6492544, essv5562917, essv5774479, essv6025216, essv6194452, essv6231149, essv6344097, essv5539435, essv6308076, essv5974468, essv6334795, essv5620614, essv6554829, essv6521547, essv6062401, essv6554544, essv6240497, essv5606715, essv5612655, essv6113412, essv5558477, essv6280223, essv6521042, essv5723683, essv6045628, essv5844101, essv5480385, essv5497322, essv6309872, essv6072469, essv6561669, essv6526095, essv5684560, essv5598419, essv5459733, essv5880732, essv5991840, essv5753588, essv6144882, essv6426056, essv5534105, essv5810552, essv5687148, essv6011308, essv6190469, essv5457241, essv6054675, essv6227892, essv6307371, essv6105951, essv6504252, essv5951453, essv5792446, essv5638517, essv6388272, essv5620870, essv6017801, essv5690676, essv6222288, essv6428263, essv6437404, essv6230296, essv5978709, essv6128980, essv6229092, essv5968001, essv6008359, essv5835756, essv5795466, essv6379981, essv5868193, essv5440792, essv6561013, essv6424990, essv5607778, essv6346533, essv5820893, essv5917236, essv6363286, essv6413727, essv6311632, essv5875183, essv5661587, essv5933527, essv6577214, essv6348118, essv5842856, essv6348656, essv6548208, essv6529813, essv5508186, essv6148189, essv5741541, essv5533031, essv6402298, essv5742441, essv6014334, essv6048269, essv5800134, essv5825865, essv6045700, essv6114321, essv5557156, essv6171213, essv5936803, essv6285546, essv5839140, essv6498119, essv6598416, essv6510435, essv6336949, essv5635107, essv5647924, essv5523236, essv5604397, essv6247802, essv6390239, essv6069617, essv5638782, essv6119817, essv5962991, essv5713877, essv6246417, essv5714646, essv5595587, essv5906171, essv5851070 | | Samples | HG00593, HG00626, HG00403, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00361, HG00524, HG00187, HG00315, HG00318, HG00181, HG00699, HG00566, HG00179, HG00449, HG00177, HG00654, HG00337, HG00327, HG00271, HG00663, HG00589, HG00272, HG00501, HG00702, HG00689, HG00448, HG00173, HG00330, HG00634, HG00610, HG00346, HG00334, HG00185, HG00537, HG00311, HG00590, HG00512, HG00281, HG00683, HG00325, HG00534, HG00422, HG00705, HG00309, HG00182, HG00427, HG00338, HG00326, HG00178, HG00323, HG00530, HG00419, HG00464, HG00543, HG00313, HG00188, HG00560, HG00629, HG00443, HG00268, HG00266, HG00183, HG00176, HG00282, HG00596, HG00557, HG00328, HG00428, HG00190, HG00653, HG00577, HG00657, HG00436, HG00556, HG00320, HG00533, HG00583, HG00344, HG00500, HG00275, HG00619, HG00708, HG00635, HG00324, HG00284, HG00273, HG00651, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG00613, HG00321, HG00276, HG00463, HG00611, HG00476, HG00336, HG00625, HG00565, HG00353, HG00580, HG00375, HG00278, HG00473, HG00607, HG00319, HG00662, HG00418, HG00620, HG00339, HG00269, HG00707, HG00672, HG00614, HG00513, HG00578, HG00478, HG00421, HG00329, HG00656, HG00342, HG00310, HG00280, HG00343, HG00377, HG00372, HG00274, HG00595, HG00472, HG00628, HG00171, HG00345, HG00180, HG00437, HG00581 | | Known Genes | | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2669581
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 144 | | Observed Complex | 0 | | Frequency | n/a |
|
|
