Variant DetailsVariant: esv2659146 Internal ID | 9578565 | Landmark | | Location Information | | Cytoband | Xq28 | Allele length | Assembly | Allele length | hg38 | 13124 | hg19 | 13124 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6435293, essv5516559, essv5585872, essv6463152, essv6015032, essv5839117, essv5700070, essv5635125, essv6435753, essv5912597, essv5777822, essv6199916, essv5857328, essv5790377, essv5696849, essv5484788, essv6243840, essv6171527, essv6017955, essv5875113, essv6250976, essv5919400, essv5626314, essv5748309, essv5458868, essv5712276, essv5696202, essv5432850, essv5612682, essv6020772, essv5567591, essv5547708, essv6204856, essv6204258, essv5456348, essv6583965, essv6401501, essv6491046, essv6422751, essv5526758, essv6283919, essv5603884, essv5775132, essv6205658, essv5586638, essv6566773, essv6155328, essv5588427, essv6055151, essv5534846, essv6202311, essv5408437, essv6500757, essv6395145, essv5796387, essv5823681, essv5913239, essv5727212, essv5681201, essv6142803, essv6329259, essv5646334, essv6181115, essv6517380, essv5767147, essv6082806, essv5546994, essv5399417, essv6349823, essv6275735, essv5621695, essv6439648, essv6486058, essv6205771, essv5925000, essv6558862, essv6067343, essv6582600, essv6245480, essv5701368, essv5792178, essv6349931, essv5893322, essv5705094, essv6120666, essv6127292, essv6056450, essv5470761, essv6126787, essv6166889, essv6234387, essv5553322, essv6535559, essv6047513, essv5778034, essv6359993, essv5802508, essv5881570, essv6073298, essv5673563, essv5922991, essv6437778, essv5771351, essv5871800, essv6292958, essv6498353, essv6013129, essv6264636, essv5659914 | Samples | HG01060, HG00189, HG01173, HG01521, HG00536, HG00231, HG00249, HG00671, HG00242, HG00559, HG00524, NA12273, HG00306, HG00566, HG00179, HG01518, HG00177, NA18602, HG01522, HG01140, HG00693, HG00337, HG00327, HG01350, HG00589, HG00251, NA20589, HG00702, HG00689, HG00448, HG00330, HG00610, HG00346, HG00270, HG00334, HG00185, HG01134, HG00281, HG00139, HG00277, HG00683, HG01519, HG01072, HG00422, HG00309, HG00182, HG00118, HG00338, HG00178, NA20818, HG01353, HG00313, HG01136, HG00154, HG00560, HG00176, HG01171, HG00282, HG00557, HG00328, HG00657, HG01515, HG00584, HG00583, HG00344, HG00500, HG00275, NA12718, HG01149, HG00324, HG00250, NA18626, HG00690, HG00404, HG00479, HG00331, HG00525, NA19682, HG00463, NA19675, HG00258, HG00285, HG00265, HG00625, NA18628, HG00375, HG00357, HG01174, HG00237, HG01137, NA19085, HG00620, HG00125, NA19078, HG00513, HG00329, HG00342, HG00174, NA19780, HG00343, HG00252, HG00595, HG01125, HG00171, NA18623, HG00554, HG01061, NA20509, HG01516 | Known Genes | TMLHE | 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) | esv2659146
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 109 | Observed Complex | 0 | Frequency | n/a |
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