Variant DetailsVariant: esv3596953 Internal ID | 6637223 | Landmark | | Location Information | | Cytoband | 3p11.1 | Allele length | Assembly | Allele length | hg38 | 24572 | hg19 | 24572 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv11068854, essv11068780, essv11068844, essv11068809, essv11068821, essv11068778, essv11068815, essv11068772, essv11068841, essv11068795, essv11068787, essv11068766, essv11068827, essv11068865, essv11068820, essv11068769, essv11068798, essv11068851, essv11068806, essv11068868, essv11068859, essv11068864, essv11068853, essv11068863, essv11068804, essv11068817, essv11068763, essv11068805, essv11068771, essv11068816, essv11068784, essv11068799, essv11068783, essv11068774, essv11068802, essv11068819, essv11068792, essv11068847, essv11068776, essv11068850, essv11068788, essv11068867, essv11068871, essv11068768, essv11068862, essv11068845, essv11068810, essv11068790, essv11068839, essv11068833, essv11068781, essv11068874, essv11068801, essv11068773, essv11068846, essv11068818, essv11068824, essv11068861, essv11068858, essv11068797, essv11068786, essv11068764, essv11068823, essv11068869, essv11068807, essv11068840, essv11068873, essv11068842, essv11068777, essv11068825, essv11068803, essv11068849, essv11068767, essv11068838, essv11068831, essv11068828, essv11068826, essv11068782, essv11068785, essv11068836, essv11068855, essv11068870, essv11068793, essv11068789, essv11068857, essv11068830, essv11068832, essv11068848, essv11068860, essv11068796, essv11068800, essv11068811, essv11068852, essv11068808, essv11068779, essv11068791, essv11068814, essv11068775, essv11068813, essv11068765, essv11068822, essv11068794, essv11068872, essv11068837, essv11068770, essv11068843, essv11068856, essv11068835, essv11068812, essv11068834, essv11068829, essv11068866 | Samples | NA19648, HG01521, HG03960, HG01860, HG01052, HG03687, NA20514, NA11920, HG01280, HG02231, HG03589, HG01389, HG00181, HG01704, HG01522, NA19746, HG01350, HG01682, HG01702, HG01351, NA20774, NA20317, HG01492, HG04070, HG01510, HG00311, NA12761, HG01067, HG00632, NA20775, NA11932, HG01527, HG01673, HG04020, HG00253, NA20755, NA20318, HG01312, HG01164, NA19007, HG00313, HG01784, NA20904, HG03785, NA20800, HG00266, HG00245, HG01669, HG01515, NA20810, HG00368, HG01612, HG01768, HG01880, HG01675, NA18630, HG02221, HG01390, HG01102, HG00273, HG01414, HG01536, NA11894, HG04173, HG04155, HG01613, HG04017, HG00140, HG01474, HG01403, HG03755, NA18536, HG01204, HG01530, HG03238, HG01190, HG00336, HG01131, HG00366, HG00353, HG02682, HG01800, HG01685, HG01362, HG01874, NA20527, HG01866, NA20778, NA19679, HG01620, HG02188, HG02371, NA19818, HG01785, HG02700, HG01765, HG01935, NA20849, NA19779, HG00342, HG01085, NA11843, NA20758, NA20528, NA19661, HG01672, NA20827, HG03931, HG01097, HG01786, HG01747, NA20511 | Known Genes | EPHA3 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3596953
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 112 | Observed Complex | 0 | Frequency | n/a |
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