Variant DetailsVariant: esv2670415 | Internal ID | 9936520 | | Landmark | | | Location Information | | | Cytoband | 7p14.3 | | Allele length | | Assembly | Allele length | | hg38 | 1690 | | hg19 | 1690 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6459940, essv5678693, essv6085133, essv5872652, essv6117491, essv5399005, essv6029025, essv6364752, essv6322076, essv5759247, essv6500112, essv6214685, essv6217567, essv5628097, essv6551889, essv6573425, essv5888959, essv5560922, essv6508336, essv5918123, essv6156314, essv6430183, essv5589816, essv5687841, essv6152930, essv5727770, essv6380650, essv6405149, essv6050090, essv6145192, essv6231929, essv6057143, essv5558220, essv6060101, essv6076416, essv5518711, essv5563700, essv6444134, essv5586925, essv6081720, essv5635017, essv6461493, essv5551631, essv5711897, essv5613815, essv6533226, essv6300974, essv5424503, essv5837903, essv5689675, essv6120742, essv6236781, essv5570583, essv5806100, essv6146404, essv6579369, essv6198319, essv6511935, essv5486035, essv5645025, essv6385482, essv5988177, essv6285961, essv5970252, essv5810836, essv5700709, essv6126395, essv6282937, essv6596843, essv5911642, essv6021063, essv6152588, essv5504240, essv5832855, essv5806508, essv6052097, essv6316761, essv6398698, essv6267547, essv6340770, essv6486851, essv6242842, essv5779530, essv5975763, essv6422907, essv6028586, essv6191939, essv5416183, essv5963568, essv5951675, essv5615055, essv5484284, essv6010759, essv5898949, essv5572625, essv6293170, essv5876856, essv6009259, essv6270184, essv6222048, essv5768466, essv6297411, essv5588674, essv6488867, essv5896306, essv5612288, essv5466590, essv5610746, essv5723696, essv5790750, essv6526421, essv5518319, essv5873350, essv6290193, essv6110677 | | Samples | HG00189, NA18621, HG00361, HG00559, HG01052, HG00187, NA18565, HG01389, HG00367, HG00699, NA18606, HG00179, HG00449, HG01051, NA18633, HG00337, HG00327, HG00271, NA18563, HG00272, HG00501, NA18982, NA18558, HG00330, HG00610, NA18582, HG00369, HG00334, HG00277, HG00236, HG00325, HG01072, NA18560, NA18617, HG00422, HG00309, HG00427, HG00530, NA18539, NA18638, HG00260, NA18544, NA18605, HG00443, NA18538, HG00266, HG00176, HG00282, HG00557, HG00328, HG00190, HG00653, HG00577, HG00475, NA19663, HG00556, HG00320, HG00344, NA18637, NA18579, NA18534, HG00692, NA18548, NA18537, HG00324, HG00373, HG00531, HG00479, HG00684, HG00613, HG00321, HG00463, NA18536, HG00246, NA18634, NA18593, NA19675, NA18541, NA18608, NA18632, HG00476, HG00285, NA18564, HG00353, NA18628, HG00136, HG00473, HG00256, NA19085, NA18615, NA18610, HG00339, NA19078, HG00707, HG00614, HG00478, HG00342, HG00174, NA18609, HG00310, HG00186, HG00112, HG00280, HG00377, HG00372, HG00274, HG00472, HG00171, HG00345, HG00554, NA18612, NA18549, HG00180, HG00437, NA19676 | | Known Genes | CCDC129 | | 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) | esv2670415
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 115 | | Observed Complex | 0 | | Frequency | n/a |
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