Variant DetailsVariant: esv2656455 | Internal ID | 9922560 | | Landmark | | | Location Information | | | Cytoband | Xq21.31 | | Allele length | | Assembly | Allele length | | hg38 | 1961 | | hg19 | 1961 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6064378, essv5656287, essv5953033, essv5782375, essv6301616, essv6132491, essv6387293, essv6121314, essv5663772, essv6400789, essv6297294, essv5852255, essv6135001, essv5957221, essv5775275, essv6107970, essv5413820, essv6201579, essv6160859, essv6274736, essv6126831, essv6525536, essv6565586, essv6271341, essv6001533, essv6443318, essv5512736, essv6344522, essv5661041, essv6192068, essv6186290, essv6012708, essv6175583, essv5457324, essv5451434, essv5859601, essv5919158, essv5632239, essv6034887, essv5575224, essv5409888, essv5900126, essv6203486, essv5534308, essv5450753, essv5907213, essv5866221, essv5657161, essv5581906, essv6548857, essv5634415, essv5811014, essv5922866, essv5689839, essv6201713, essv5465761, essv6140740, essv5568297, essv6151855, essv6173103, essv5485659, essv6527866, essv5659959, essv5990335, essv5558394, essv5825368, essv6516916, essv5609758, essv6124311, essv6427646, essv6184810, essv5486973, essv6057849, essv5666743, essv6034969, essv6025695, essv5855686, essv6257046, essv5460746, essv5587057, essv5828654, essv6002431, essv5520973, essv5614945, essv6401645, essv6538473, essv5518161, essv5586440, essv5950483, essv5600055, essv6275943, essv5837559, essv6263690, essv5976592, essv5874174, essv6010088, essv6387323, essv5466974, essv6530882, essv6219590, essv6469319, essv6432397, essv5628101, essv5759030, essv5529417, essv6243273, essv5751093, essv5870577, essv5833028, essv5877616, essv5954225, essv6544368, essv6400173, essv5569540, essv5673856, essv5945918, essv6047275, essv5729518, essv5670942, essv5585004, essv5506834, essv6096213, essv6347922 | | Samples | NA12383, HG00114, NA19701, HG01441, HG00650, NA12717, NA11830, NA20529, HG00143, HG00231, NA20766, HG00249, NA11995, HG00242, HG00306, NA20802, HG00367, NA19684, NA12058, NA20808, HG00177, NA19443, NA12400, NA12155, HG01522, NA12413, HG00337, HG00138, NA19660, HG01070, HG00251, HG00122, NA20586, NA20774, HG01168, NA20756, NA20317, NA12891, NA12348, HG00736, HG01083, HG00247, HG00158, HG01069, HG01067, HG00335, HG00148, HG00106, NA20819, NA20812, HG00325, HG00705, NA18986, NA12889, HG00118, HG01198, HG00338, HG01048, HG00178, NA20533, HG00419, HG00264, NA11993, HG00464, HG00313, HG00133, HG01183, HG00154, HG00149, NA18605, NA18613, HG00268, HG00266, HG01171, HG00282, NA19056, HG00245, NA12342, NA12878, HG00190, HG01095, NA20536, NA12718, NA19776, HG00740, HG01073, NA12249, NA06989, NA12827, HG00276, HG00146, NA20828, HG00126, NA12716, HG00285, NA19749, NA20815, HG00638, NA19380, NA20785, HG01357, HG01174, HG00098, HG00237, NA18610, HG01489, HG00620, HG00125, HG00111, NA12749, HG01055, HG00123, NA20510, HG00112, NA20807, HG00343, NA18983, HG00377, HG00252, HG00171, HG01191, HG00180, HG00553 | | Known Genes | PCDH11X | | 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) | esv2656455
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 123 | | Observed Complex | 0 | | Frequency | n/a |
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