Variant DetailsVariant: esv2674966 | Internal ID | 9941071 | | Landmark | | | Location Information | | | Cytoband | 3q27.3 | | Allele length | | Assembly | Allele length | | hg38 | 1939 | | hg19 | 1939 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6554018, essv5964054, essv5791778, essv6221819, essv5844198, essv5469713, essv6028662, essv5670390, essv6223996, essv6155026, essv5514565, essv5442623, essv6371168, essv5452067, essv6280982, essv6584449, essv6256037, essv5423014, essv5549931, essv5729252, essv5633070, essv5526428, essv6585459, essv6242392, essv6036518, essv6255274, essv6262020, essv5855892, essv6400305, essv5931029, essv5899524, essv6493242, essv5713705, essv5973836, essv5467476, essv6277187, essv6333197, essv5777308, essv6377954, essv6290728, essv6021286, essv5923311, essv5660238, essv6434254, essv6397088, essv5928531, essv5663340, essv5981235, essv6512600, essv5546133, essv5969842, essv5621829, essv6244958, essv5663174, essv5677497, essv5450164, essv5443431, essv6189163, essv6268769, essv5586354, essv5692675, essv5761063, essv5963265, essv6367572, essv5447082, essv6253207, essv5848514, essv6427545, essv5752010, essv5962333, essv5968717, essv6492190, essv6194752, essv6438654, essv5599593, essv5790705, essv5772796, essv6021296, essv6150401, essv5616400, essv6086189, essv6472679, essv5906711, essv6397501, essv6123608, essv5420654, essv5669263, essv5684017, essv6049556, essv5580204, essv6368641, essv6011204, essv6206167, essv6273674, essv5864706, essv6414879, essv5924130, essv5857663, essv5854236, essv5716809, essv6203182, essv6178810, essv6134641, essv6289922, essv5666755, essv5771398, essv6444257, essv6174458, essv6117767, essv6177175, essv5940335, essv6593746, essv6214215, essv5539299, essv5838099, essv5672926, essv5510407, essv5723267, essv6036603, essv5864247, essv6048291, essv6574717, essv6575459, essv6469163, essv6118034, essv6036969, essv5952745, essv6079288, essv5726617, essv5419574, essv5757587, essv6375249, essv6032955, essv5657712, essv6367339, essv5844546, essv6133499, essv5572133, essv6576265, essv6143148, essv6006879, essv6230802, essv5474956, essv6192901, essv6125495, essv5916799, essv6253540, essv6381348, essv5829667, essv5399157, essv6506103, essv5683598, essv6386750, essv6577285, essv5834951, essv6124298, essv5991335, essv6515905, essv5490239, essv5956279, essv6161146, essv5543789, essv6351042, essv6350617, essv5462864, essv5601598 | | Samples | NA12383, HG00542, HG00143, HG00536, NA19397, HG00608, NA11829, NA19066, NA18508, HG00559, NA19399, NA12273, HG00187, HG01079, HG00100, NA11931, HG01389, HG00306, HG00151, NA20532, NA19350, HG00699, NA18545, NA19819, NA19777, NA18596, NA12340, HG00566, NA18530, NA12058, HG00449, HG00177, HG01461, NA12400, NA18633, HG00261, NA07357, NA18602, NA18988, NA18627, NA12341, NA12813, HG00663, NA19068, HG00641, NA19396, HG00272, NA18597, NA18489, NA20798, NA19762, HG01351, NA19448, HG01167, NA18635, NA19062, NA18574, NA07048, HG00346, NA19771, NA12287, HG01083, NA18949, NA18611, NA12761, HG01069, HG01080, HG01067, HG00325, NA19719, NA18560, NA11994, NA19075, HG00422, NA19471, HG01176, NA18986, NA19722, HG00338, NA18985, HG00323, NA18867, HG00253, NA19921, NA18638, HG00264, NA20753, NA10847, HG00313, HG00133, HG00154, HG00560, NA18613, NA18538, HG01171, HG01384, HG00245, HG00428, NA19462, NA12878, HG00732, NA20536, NA19663, HG00533, HG01498, HG00500, HG00263, NA19788, HG00275, HG00708, NA19064, HG01047, NA18566, HG00324, HG01073, HG00373, HG00684, HG01101, HG00140, NA18553, NA12827, NA19761, NA19682, NA18536, NA19012, NA19729, NA18632, HG00336, NA18952, NA12775, HG00565, HG00366, NA18950, NA19732, NA19435, NA18941, HG00638, HG00278, NA20785, NA20803, NA19783, HG00662, NA19085, NA06986, HG00339, NA19078, NA19472, HG00329, HG00342, HG00267, HG00174, HG00123, NA20510, HG00186, HG00112, NA19770, NA18983, NA19661, NA18989, NA11892, NA19755, HG01082, HG00554, HG01191, NA12776, NA18577 | | Known Genes | | | 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) | esv2674966
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 166 | | Observed Complex | 0 | | Frequency | n/a |
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