Variant DetailsVariant: esv2672632 | Internal ID | 9938737 | | Landmark | | | Location Information | | | Cytoband | 7q21.3 | | Allele length | | Assembly | Allele length | | hg38 | 333 | | hg19 | 333 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6441154, essv5927351, essv6585562, essv6535203, essv5505024, essv6129428, essv5909384, essv5615651, essv5754971, essv6096002, essv6218398, essv6592412, essv6329842, essv5999942, essv5481921, essv6491238, essv6506410, essv5647775, essv6240711, essv5438504, essv5840669, essv5594160, essv5496702, essv5733691, essv5490054, essv6097783, essv5920928, essv5589673, essv6421273, essv6544403, essv6307939, essv6380020, essv5439094, essv6299253, essv6411295, essv5798632, essv5700211, essv6467026, essv5728561, essv5737131, essv5738968, essv6259680, essv6349332, essv5767786, essv5526181, essv6393663, essv5937224, essv6116201, essv5458827, essv5789479, essv6577674, essv5956205, essv5768171, essv5883381, essv5662240, essv6518404, essv5420687, essv5673870, essv5703479, essv5439437, essv5425313, essv6463842, essv6251495, essv5965381, essv6070370, essv5694809, essv6449742, essv6012822, essv5856631, essv6450599, essv6420851, essv5445809, essv6237275, essv5806115, essv6119147, essv5608429, essv5600094, essv5441334, essv5645718, essv5467447, essv6233336, essv5608296, essv6293960, essv5606746, essv5667664, essv6116751, essv5430968, essv6157062, essv5633737, essv5545790, essv5500396, essv5797012, essv5927776, essv6383115, essv6557608, essv6155546, essv6489380, essv6178404, essv6134095, essv6147498, essv6418184, essv5817940, essv6013755, essv6400684, essv6284633, essv5752276, essv5872145, essv5828010, essv6028139, essv6580369, essv5425235, essv6455511, essv6076991, essv5396631, essv5500302, essv6425349, essv6049550, essv5470671, essv6431984, essv6289691, essv5813052, essv6304618, essv5886016, essv5528282, essv6507445, essv6546287, essv5747300, essv5714707, essv6088826, essv5448474, essv6257101, essv6571151, essv6538252, essv6345005, essv5703420, essv5851158, essv5500342, essv6074601, essv6463799, essv6583441, essv6004846, essv5756293, essv6482449, essv5907720, essv6193778, essv6049560, essv6004808, essv5630192, essv6221060, essv6379466 | | Samples | HG00114, HG00592, NA19703, NA19055, HG00536, NA18861, NA10851, HG01359, HG00524, HG01052, HG00187, NA12843, NA11920, NA18599, HG00315, NA12045, HG00640, HG00318, HG00244, NA20294, NA18545, NA19684, NA12058, NA18959, HG00177, HG00150, NA19190, NA07357, NA19067, HG00693, NA18627, HG00271, NA20814, NA19446, NA19171, NA19379, HG00501, HG00122, NA19678, HG01488, HG00689, NA20586, NA20756, NA18567, NA12891, NA18547, NA18960, NA18942, NA19062, NA11918, NA12283, NA20540, HG00185, NA18964, NA18611, HG00281, NA20759, HG00277, NA12005, NA18977, NA19372, NA19731, HG00534, NA18986, NA19087, NA12889, HG00182, NA19002, HG00159, NA18557, HG00323, NA18973, NA20515, NA20755, NA18539, NA18638, HG00108, NA19007, NA11831, NA10847, HG00313, NA20535, NA19210, HG00731, HG00176, HG00282, HG00557, NA20505, NA12003, NA12878, NA18956, NA20810, NA19391, NA19455, NA20314, NA18516, HG00436, HG00556, HG00533, HG00275, NA18572, NA18948, NA19064, HG01390, HG00284, NA19084, HG00404, HG01383, NA12892, HG00525, HG00321, HG00140, NA19059, NA20828, HG00463, NA18536, NA12778, NA18541, NA18953, NA19375, HG00476, NA18961, HG00353, NA19072, NA18950, HG00375, NA20804, NA19144, HG00607, NA20504, NA19360, HG00125, NA19759, HG00614, HG00578, NA18971, HG01491, HG00312, NA18983, HG00372, HG00472, NA19755, NA18968, NA19063, HG01191, HG01437, HG00581, NA18965, NA18577, NA20509 | | Known Genes | ASNS | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2672632
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 150 | | Observed Complex | 0 | | Frequency | n/a |
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