Variant DetailsVariant: esv3621498 | Internal ID | 7008367 | | Landmark | | | Location Information | | | Cytoband | 9q31.3 | | Allele length | | Assembly | Allele length | | hg38 | 1020 | | hg19 | 1020 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv13602911, essv13602836, essv13602949, essv13602820, essv13602779, essv13602970, essv13602866, essv13602802, essv13602978, essv13602893, essv13602869, essv13602783, essv13602847, essv13602951, essv13602910, essv13602862, essv13602839, essv13602834, essv13602969, essv13602844, essv13602954, essv13602851, essv13602784, essv13602801, essv13602904, essv13602895, essv13602983, essv13602896, essv13602952, essv13602919, essv13602880, essv13602964, essv13602907, essv13602827, essv13602967, essv13602926, essv13602864, essv13602856, essv13602965, essv13602901, essv13602790, essv13602972, essv13602973, essv13602872, essv13602956, essv13602874, essv13602807, essv13602823, essv13602955, essv13602945, essv13602977, essv13602934, essv13602903, essv13602933, essv13602883, essv13602908, essv13602931, essv13602909, essv13602915, essv13602971, essv13602871, essv13602858, essv13602809, essv13602816, essv13602798, essv13602852, essv13602781, essv13602840, essv13602835, essv13602789, essv13602899, essv13602837, essv13602884, essv13602863, essv13602791, essv13602838, essv13602877, essv13602848, essv13602968, essv13602958, essv13602923, essv13602785, essv13602882, essv13602811, essv13602898, essv13602792, essv13602815, essv13602812, essv13602804, essv13602879, essv13602855, essv13602774, essv13602960, essv13602800, essv13602937, essv13602845, essv13602975, essv13602797, essv13602826, essv13602938, essv13602985, essv13602921, essv13602870, essv13602796, essv13602859, essv13602939, essv13602936, essv13602787, essv13602943, essv13602928, essv13602873, essv13602814, essv13602897, essv13602959, essv13602982, essv13602914, essv13602775, essv13602865, essv13602788, essv13602841, essv13602887, essv13602878, essv13602821, essv13602773, essv13602981, essv13602808, essv13602776, essv13602889, essv13602833, essv13602817, essv13602824, essv13602894, essv13602794, essv13602892, essv13602885, essv13602832, essv13602799, essv13602976, essv13602932, essv13602890, essv13602986, essv13602846, essv13602849, essv13602795, essv13602957, essv13602850, essv13602935, essv13602962, essv13602786, essv13602825, essv13602924, essv13602886, essv13602918, essv13602984, essv13602913, essv13602810, essv13602927, essv13602853, essv13602813, essv13602875, essv13602979, essv13602925, essv13602843, essv13602944, essv13602828, essv13602963, essv13602948, essv13602867, essv13602818, essv13602778, essv13602929, essv13602831, essv13602857, essv13602819, essv13602980, essv13602881, essv13602829, essv13602906, essv13602842, essv13602900, essv13602920, essv13602950, essv13602946, essv13602780, essv13602987, essv13602941, essv13602940, essv13602974, essv13602966, essv13602805, essv13602961, essv13602891, essv13602876, essv13602917, essv13602860, essv13602912, essv13602930, essv13602916, essv13602947, essv13602854, essv13602905, essv13602803, essv13602942, essv13602822, essv13602868, essv13602861, essv13602782, essv13602922, essv13602777, essv13602830, essv13602793, essv13602888, essv13602953, essv13602902, essv13602806 | | Samples | NA18998, HG01985, HG01850, HG00542, HG02072, HG01965, HG00536, HG00608, NA18947, HG00384, NA19066, HG01855, HG02026, HG03589, HG00457, HG00306, NA18603, NA18528, HG03616, HG01802, HG00452, HG02050, HG00566, NA18959, HG03667, HG02271, HG00737, HG00879, HG02154, NA18526, HG01809, HG04156, HG00693, NA18988, NA18627, HG04059, HG00622, NA19089, NA19076, HG02153, HG02185, HG02407, HG02069, HG01853, HG02140, HG02156, HG00599, HG00448, NA21130, HG02383, HG02155, NA18635, NA18567, HG01968, NA18993, HG00458, HG02266, NA18942, NA18618, HG01816, NA18574, HG03874, HG02299, HG02655, NA18582, NA20540, NA19088, NA18571, HG01063, HG02733, HG01840, HG01982, NA18949, HG01859, HG00590, NA18611, NA18749, HG03619, NA18970, HG02395, HG03986, HG02512, HG02067, NA18977, HG02389, HG03888, HG00534, NA19002, HG00406, NA19725, HG02073, NA18557, HG03832, NA18973, NA18539, HG00675, NA18648, HG03862, HG01942, NA20818, HG00543, HG02402, HG02166, NA18613, HG01248, HG02136, HG00443, NA18538, HG01841, HG01797, HG00596, HG03007, HG00557, NA19086, HG02397, HG00657, HG01938, HG00475, HG02084, HG00556, HG00533, NA19081, HG04035, HG02522, NA20767, HG01029, NA18981, NA21116, NA18548, NA18537, NA18566, NA19000, NA19084, HG00844, HG00690, HG01197, HG02121, NA18946, HG02141, NA18532, HG04017, HG03854, HG02601, NA19009, HG02184, NA18963, HG00704, HG02286, HG00463, HG04118, HG00410, HG02408, HG02399, NA18945, NA18541, NA19003, NA20872, NA20522, HG02089, HG00625, HG02049, HG03708, HG02088, HG00565, HG04239, HG02682, NA18950, HG01800, NA19010, NA12046, NA20902, NA18629, HG00116, NA07037, HG02019, HG00662, NA19085, HG02188, HG01862, HG02181, HG03729, NA19078, HG00513, HG02367, HG01804, HG01028, HG03863, HG01846, HG02392, HG02116, HG00123, HG01799, NA18609, HG00234, HG02182, NA19080, HG03872, NA18552, HG02348, HG01794, HG00595, NA18984, HG00472, NA18989, HG02020, HG01863, HG04161, HG00759, NA18623, HG01869, NA19063, HG02406, HG01191, HG00978, HG00437 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3621498
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 215 | | Observed Complex | 0 | | Frequency | n/a |
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