Variant DetailsVariant: esv3638077 Internal ID | 6678175 | Landmark | | Location Information | | Cytoband | 16p12.3 | Allele length | Assembly | Allele length | hg38 | 4067 | hg19 | 4067 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15390821, essv15390876, essv15390800, essv15390830, essv15390809, essv15390765, essv15390760, essv15390869, essv15390844, essv15390788, essv15390753, essv15390813, essv15390750, essv15390762, essv15390834, essv15390797, essv15390820, essv15390825, essv15390808, essv15390744, essv15390773, essv15390770, essv15390769, essv15390738, essv15390756, essv15390853, essv15390817, essv15390793, essv15390829, essv15390783, essv15390880, essv15390741, essv15390751, essv15390864, essv15390872, essv15390822, essv15390828, essv15390879, essv15390818, essv15390865, essv15390805, essv15390866, essv15390871, essv15390836, essv15390758, essv15390833, essv15390768, essv15390772, essv15390859, essv15390796, essv15390874, essv15390831, essv15390875, essv15390824, essv15390807, essv15390867, essv15390846, essv15390790, essv15390841, essv15390745, essv15390870, essv15390848, essv15390827, essv15390816, essv15390747, essv15390743, essv15390878, essv15390837, essv15390742, essv15390804, essv15390787, essv15390852, essv15390799, essv15390757, essv15390826, essv15390801, essv15390835, essv15390798, essv15390740, essv15390855, essv15390881, essv15390777, essv15390748, essv15390882, essv15390815, essv15390784, essv15390761, essv15390752, essv15390850, essv15390842, essv15390776, essv15390860, essv15390792, essv15390779, essv15390755, essv15390838, essv15390810, essv15390802, essv15390819, essv15390785, essv15390782, essv15390839, essv15390811, essv15390794, essv15390746, essv15390795, essv15390832, essv15390861, essv15390806, essv15390759, essv15390775, essv15390851, essv15390780, essv15390845, essv15390789, essv15390774, essv15390739, essv15390862, essv15390823, essv15390863, essv15390791, essv15390857, essv15390786, essv15390749, essv15390766, essv15390781, essv15390771, essv15390764, essv15390814, essv15390858, essv15390856, essv15390877, essv15390873, essv15390767, essv15390847, essv15390778, essv15390849, essv15390854, essv15390868, essv15390812, essv15390803, essv15390843, essv15390763, essv15390840, essv15390754 | Samples | HG00403, NA19058, HG02250, HG01965, HG02002, HG01438, HG00671, NA19066, HG02026, NA20274, HG00766, HG02122, HG02029, NA18979, HG01066, HG02277, HG01486, HG02058, HG02050, HG01947, NA18633, HG00663, HG02312, HG02153, HG01070, HG02151, NA19728, NA18995, HG02105, NA18595, HG02383, HG03937, NA18619, HG01843, HG01599, HG02374, HG01840, HG01859, NA18611, NA19651, HG00632, HG02067, NA18617, HG02178, HG01844, HG01198, NA18975, HG03832, HG01967, HG00743, HG00464, HG02402, HG00560, NA18613, HG00629, HG01847, HG01867, HG01841, HG00982, NA19070, NA19056, NA18525, HG01797, HG02025, NA18956, NA18644, HG02397, HG00701, HG02084, HG00436, HG00556, HG02390, HG01845, NA19081, NA19788, NA18534, HG00619, NA19064, NA18537, HG02364, NA20299, HG00844, HG00404, HG00531, HG01197, HG02121, HG02086, HG01130, HG00613, HG00525, HG01842, NA19009, NA18963, NA18536, HG03991, HG00864, NA18570, HG00410, NA18634, HG01107, NA18541, NA19012, NA18978, NA19652, HG02089, NA18535, HG01597, HG01980, HG02088, HG01362, NA18941, HG01874, NA19090, HG01939, HG01977, HG00473, HG02179, HG01951, HG01798, NA18943, NA19085, HG04141, HG00707, HG00614, HG02401, HG02367, NA19779, HG00421, NA18987, HG02113, HG03615, HG01817, NA18552, HG01794, HG01464, NA18989, HG02020, NA18623, HG02351, HG02406, NA19074, HG00437, NA18562, NA18965, NA18620 | Known Genes | XYLT1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638077
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 145 | Observed Complex | 0 | Frequency | n/a |
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