Variant DetailsVariant: esv2667866 | Internal ID | 9933971 | | Landmark | | | Location Information | | | Cytoband | Xq26.3 | | Allele length | | Assembly | Allele length | | hg38 | 116 | | hg19 | 116 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5869111, essv6322656, essv5855216, essv6478420, essv5505464, essv5639208, essv5472403, essv6521555, essv6413806, essv6101857, essv5602304, essv5620672, essv5870276, essv5407551, essv5837306, essv5524249, essv5783329, essv6451092, essv5643507, essv6592056, essv5936784, essv5759619, essv6208706, essv5922540, essv5790525, essv6291689, essv5695685, essv5659143, essv6166444, essv5549256, essv6454149, essv5969171, essv5438947, essv5952041, essv5943396, essv5885946, essv5591692, essv5799216, essv6328026, essv5858341, essv6267558, essv5950144, essv5683413, essv5545420, essv6368839, essv6544956, essv6180458, essv6455041, essv6106245, essv5768639, essv5637277, essv6175513, essv5717607, essv6217302, essv6312086, essv5613046, essv5495725, essv5786182, essv5894901, essv5629226, essv6254765, essv5491153, essv6243508, essv6216647, essv5401039, essv5448723, essv5957506, essv5707862, essv5468019, essv5928826, essv5429513, essv5426468, essv6381309, essv6347689, essv5576309, essv6152146, essv6207162, essv5646452, essv6119726, essv6423350, essv6408214, essv5797454, essv5569486, essv6373680, essv6107896, essv5940319, essv6107021, essv6470406, essv6080592, essv6419868, essv6243696, essv5918912, essv6588585, essv5568423, essv6524488, essv6293100, essv5834171, essv6150357, essv6317265, essv6158460, essv5846615, essv5921840, essv5660387, essv5813255, essv6568358, essv6471971, essv6301487, essv6298184, essv6215076, essv5935119, essv6145056, essv6216398, essv6432140, essv6483494, essv5735527, essv5494584, essv5689954, essv5926095, essv6196391, essv5680919, essv6045159, essv6266141, essv6223330, essv6452658, essv6446706, essv5704440, essv6376551, essv5918235, essv5990949, essv5532267, essv5785595, essv6370062, essv6107422, essv5912634, essv5825261, essv6304719, essv6127123, essv6011790, essv6449852, essv6412174, essv6004521, essv6136164, essv5585560, essv5569690, essv6183720, essv5816984, essv6287450, essv5549438, essv5843505, essv5550515, essv5396494, essv6530889, essv5894437, essv6040171, essv6391916, essv5604233, essv5774421, essv5547286 | | Samples | NA12383, HG00650, NA19648, NA12842, HG01462, HG00608, HG00142, NA20766, NA18947, NA19066, NA20514, HG00257, HG00315, HG00306, HG00233, NA12045, HG01465, NA18545, NA12004, NA18596, NA18530, NA18959, NA18606, HG00115, HG00449, NA20507, NA19190, NA18633, HG01522, HG01140, HG00337, HG00663, NA19068, HG01350, NA18550, HG01070, NA18597, NA18595, HG00702, NA18982, NA18558, NA18942, NA18618, NA11992, NA18571, HG00247, NA19054, NA18964, HG00537, NA18949, NA12761, HG00281, HG00139, NA19651, HG00236, HG00232, NA12044, HG00422, NA18986, NA19239, NA18557, HG01133, HG00323, HG00419, HG00253, NA19789, HG00264, HG00464, HG01124, NA20818, HG01353, HG00543, HG00313, HG00137, HG00154, HG00443, HG00268, HG00183, HG01171, NA19056, HG00557, HG00245, NA12342, NA20809, NA18956, HG00657, HG00320, HG00583, HG00344, HG00263, HG00275, NA18572, NA18630, HG00619, HG00692, NA18537, NA20525, HG00324, NA18573, NA19114, HG00479, HG00684, NA12892, NA18532, HG00117, HG00321, HG00140, NA18553, NA19099, HG01334, NA18555, HG00276, NA20828, NA18593, NA18541, HG01148, HG00254, NA18961, NA18952, NA18559, NA18517, NA12775, NA19240, NA12046, NA20790, HG00473, HG00237, HG00319, NA18943, NA07037, HG00256, NA06986, HG00125, NA19078, HG00111, HG00513, HG00312, NA19779, HG00123, NA18873, NA20807, NA19711, NA19900, HG00252, NA19661, NA18984, NA07056, NA18488, NA18624, NA12006, NA18623, HG01112, NA19074, HG00553, HG00437, NA18965, NA18577, NA18620 | | Known Genes | FGF13 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2667866
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 158 | | Observed Complex | 0 | | Frequency | n/a |
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