Variant DetailsVariant: esv2663159 | Internal ID | 9929264 | | Landmark | | | Location Information | | | Cytoband | 10q24.32 | | Allele length | | Assembly | Allele length | | hg38 | 1081 | | hg19 | 1081 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6585006, essv6369896, essv6500384, essv6056812, essv5775471, essv6089533, essv5703972, essv6381948, essv6441916, essv5797858, essv5608355, essv6489522, essv6458232, essv5621322, essv5676969, essv6243398, essv6567340, essv6212934, essv5700204, essv6220404, essv6012301, essv6146405, essv6417342, essv5803130, essv5995388, essv5439172, essv6279706, essv6280058, essv5658507, essv6005425, essv6100092, essv5861894, essv5718990, essv6246979, essv5640010, essv6545697, essv6072065, essv6050417, essv5446473, essv5594835, essv6257685, essv6262758, essv6070046, essv6029481, essv6195577, essv5563782, essv5937870, essv6428398, essv6572332, essv6144011, essv6299808, essv6550569, essv5889771, essv5434510, essv6356014, essv5483376, essv6559402, essv5685564, essv6089208, essv5439883, essv6259976, essv5944356, essv6219708, essv6415055, essv6136501, essv5604909, essv6353454, essv6257757, essv5994054, essv5942465, essv5784988, essv6372038, essv6283291, essv5747611, essv6131016, essv6284947, essv6025471, essv5793672, essv6158319, essv5511210, essv6190159, essv6103456, essv6547004, essv6082868, essv6276553, essv5746009, essv5669281, essv6153784, essv5759695, essv5408477, essv6543567, essv6385625, essv6070948, essv6053388, essv5858353, essv6583692, essv5580124, essv5807377, essv5846705, essv6058858, essv6346575, essv6554254, essv6253849, essv5553448, essv6055404, essv5977185, essv5902723, essv6001363, essv5997622, essv6286822 | | Samples | HG00096, NA19701, NA12717, NA19703, NA19204, NA18508, NA19399, NA19704, NA12045, HG00318, NA19092, NA18486, NA18504, NA20332, NA19684, NA19377, NA12058, HG00150, HG01461, NA19190, NA18870, NA20356, NA12399, NA20806, NA12813, NA07346, NA19396, HG00138, NA19379, NA18519, HG00251, NA19201, NA19315, NA18489, NA18923, NA19198, NA20795, NA18916, NA11918, NA07347, NA18498, NA20287, NA20336, HG00277, NA12275, NA19383, HG00236, NA19238, NA11994, NA19317, NA19189, HG00326, HG00323, HG00264, HG01124, NA11831, HG01353, HG00313, HG00188, NA19247, HG00266, NA18934, HG01384, HG00245, NA19236, NA19982, NA18871, NA20344, NA18907, HG01390, HG00273, NA18912, HG00117, NA18853, NA12827, NA20282, HG01334, NA19756, NA12778, NA19395, NA18858, NA19436, NA20296, NA19440, HG00336, NA19256, NA19712, HG00734, NA19331, HG00098, NA19334, NA20778, NA19324, NA20797, HG01342, NA12347, HG00125, NA19376, HG00513, NA19248, HG01491, NA20510, HG00310, NA18873, HG00280, NA19726, HG00274, NA19463, NA12154, NA19346 | | Known Genes | FBXW4 | | 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) | esv2663159
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 110 | | Observed Complex | 0 | | Frequency | n/a |
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