Variant DetailsVariant: esv3641604 Internal ID | 6681689 | Landmark | | Location Information | | Cytoband | 18p11.31 | Allele length | Assembly | Allele length | hg38 | 1591 | hg19 | 1591 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15779759, essv15779791, essv15779671, essv15779799, essv15779694, essv15779780, essv15779806, essv15779726, essv15779670, essv15779846, essv15779823, essv15779863, essv15779859, essv15779685, essv15779808, essv15779714, essv15779851, essv15779682, essv15779733, essv15779745, essv15779748, essv15779734, essv15779789, essv15779673, essv15779686, essv15779725, essv15779858, essv15779690, essv15779737, essv15779706, essv15779753, essv15779770, essv15779832, essv15779819, essv15779677, essv15779736, essv15779795, essv15779703, essv15779810, essv15779793, essv15779860, essv15779683, essv15779724, essv15779701, essv15779744, essv15779802, essv15779830, essv15779768, essv15779718, essv15779794, essv15779847, essv15779867, essv15779811, essv15779684, essv15779787, essv15779838, essv15779870, essv15779840, essv15779695, essv15779711, essv15779834, essv15779715, essv15779850, essv15779678, essv15779796, essv15779786, essv15779861, essv15779765, essv15779857, essv15779746, essv15779839, essv15779837, essv15779848, essv15779705, essv15779797, essv15779669, essv15779679, essv15779836, essv15779841, essv15779783, essv15779804, essv15779803, essv15779845, essv15779680, essv15779790, essv15779675, essv15779807, essv15779749, essv15779798, essv15779800, essv15779816, essv15779699, essv15779707, essv15779719, essv15779785, essv15779833, essv15779865, essv15779672, essv15779773, essv15779817, essv15779723, essv15779828, essv15779697, essv15779727, essv15779743, essv15779827, essv15779855, essv15779822, essv15779767, essv15779728, essv15779750, essv15779821, essv15779856, essv15779731, essv15779869, essv15779809, essv15779687, essv15779747, essv15779709, essv15779868, essv15779778, essv15779777, essv15779815, essv15779843, essv15779689, essv15779698, essv15779854, essv15779755, essv15779700, essv15779871, essv15779751, essv15779676, essv15779824, essv15779668, essv15779688, essv15779766, essv15779842, essv15779763, essv15779814, essv15779782, essv15779826, essv15779720, essv15779844, essv15779779, essv15779754, essv15779722, essv15779738, essv15779752, essv15779732, essv15779691, essv15779772, essv15779825, essv15779820, essv15779740, essv15779693, essv15779696, essv15779716, essv15779758, essv15779764, essv15779774, essv15779674, essv15779710, essv15779760, essv15779735, essv15779812, essv15779702, essv15779708, essv15779788, essv15779756, essv15779829, essv15779853, essv15779784, essv15779741, essv15779792, essv15779742, essv15779864, essv15779849, essv15779866, essv15779862, essv15779692, essv15779704, essv15779717, essv15779761, essv15779801, essv15779681, essv15779813, essv15779721, essv15779730, essv15779771, essv15779769, essv15779712, essv15779835, essv15779739, essv15779805, essv15779762, essv15779831, essv15779713, essv15779775, essv15779776, essv15779729, essv15779757, essv15779781, essv15779852, essv15779818 | Samples | HG02879, HG03684, NA20281, NA18621, HG00881, HG01813, HG01926, HG02250, HG02291, HG01440, NA18616, HG02275, NA18951, HG02138, NA20809, NA18534, HG02025, HG02164, NA18952, HG00705, HG02086, HG01342, NA20510, NA19310, HG00565, HG00736, HG00632, HG01800, HG01794, HG02513, NA19072, HG03295, NA19455, HG01845, HG02152, NA18603, NA18993, NA18948, HG02260, HG01085, NA19334, NA19331, NA18969, NA18972, HG02722, NA19010, HG02002, HG02884, NA18542, HG02105, HG02379, HG02314, HG00683, HG02389, HG01958, NA18994, HG02322, HG02274, NA18965, HG03380, NA19355, HG01871, HG01936, HG01841, NA18950, HG02047, HG01812, HG02982, HG02082, HG02402, HG02312, HG04238, HG02155, HG03575, NA18992, HG01392, HG00406, HG02121, NA18622, NA18960, HG01595, HG02032, NA18990, HG00689, HG02373, HG03770, NA18531, NA18592, NA19083, HG01815, NA19440, HG01556, NA18976, NA19256, NA19075, HG00451, HG00634, HG00982, NA18634, NA18643, HG00237, HG01596, HG01599, HG00662, NA18539, HG00867, HG01797, HG03063, NA19213, HG01437, HG02131, NA19785, NA18747, NA18645, NA19189, NA19759, NA19372, NA18954, HG04161, NA19024, HG00560, HG02573, NA18558, HG02017, NA19901, NA18748, NA18942, NA18961, HG02087, HG00513, HG01260, HG02384, NA21100, HG02364, HG02072, HG02536, NA19091, HG03713, HG01531, HG02180, HG02299, HG02190, NA18543, HG03028, NA18619, HG00445, NA19729, NA18907, NA19723, HG00611, HG00650, HG02154, NA18740, HG01953, HG02351, HG03045, NA18565, HG03267, HG03702, HG01862, HG02035, NA18560, NA18989, HG00118, HG03815, HG02561, NA18614, HG01802, NA19770, HG01464, NA19225, HG00656, HG02678, NA19732, HG00422, NA19006, HG01808, HG01855, HG02271, HG00623, HG02353, HG00625, HG01842, HG02136, NA18574, HG01374, HG00473, HG01631, NA19087, NA19200, NA19385, HG01976, HG04182, HG01863, HG02396, NA18519, HG03824, HG02367, HG00531, HG02512, HG02179, NA18553, HG04107, NA19439 | Known Genes | DLGAP1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3641604
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 204 | Observed Complex | 0 | Frequency | n/a |
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