Variant DetailsVariant: esv2662723 Internal ID | 9582142 | Landmark | | Location Information | | Cytoband | 10q22.1 | Allele length | Assembly | Allele length | hg38 | 2600 | hg19 | 2600 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv153e199 | Supporting Variants | essv6071737, essv6269596, essv6185000, essv6588324, essv6236016, essv5623380, essv5537997, essv5811634, essv6245014, essv6076883, essv6462366, essv5930844, essv6566683, essv5979338, essv5568941, essv5648840, essv5580542, essv6347412, essv6113442, essv6255653, essv6213098, essv6076403, essv5591241, essv5998951, essv6596343, essv5830030, essv6058828, essv5805402, essv5448908, essv5526526, essv6302220, essv5579662, essv6377866, essv6308522, essv5879578, essv6287749, essv6021481, essv5879820, essv6393853, essv5470223, essv5847104, essv5539366, essv6200464, essv5740097, essv6247501, essv6567864, essv6380503, essv6094374, essv6486541, essv5712465, essv6539497, essv6477728, essv5909465, essv5798930, essv6359505, essv5763644, essv6236561, essv6171021, essv6473753, essv5872604, essv5539162, essv5558208, essv6547337, essv6532532, essv6442827, essv6432096, essv6309542, essv6011593, essv5531529, essv6454141, essv5815689, essv5915040, essv5534763, essv5471408, essv5420652, essv5860605, essv5942767, essv5713056, essv5445571, essv5900125, essv5903862, essv5510999, essv5400443, essv6359133, essv5991324, essv6060504, essv5580701, essv6565503, essv5718664, essv6092634, essv5639452, essv5736870, essv6569864, essv6482059, essv6503506, essv5841364, essv5709647, essv5970963, essv6314990, essv6592881, essv6505970, essv5498823, essv6220699, essv6235933, essv5908877, essv5959055, essv5698265, essv6364528, essv5760532, essv6587692, essv6157813, essv6462008, essv6207375, essv6184764, essv6458411, essv6130091, essv5824062, essv5598292, essv5622055, essv6123513, essv6229274, essv6005272, essv6516831, essv6450966, essv5956081, essv6240986, essv5775029, essv5421759, essv5522884, essv5942935, essv6272523, essv6490571, essv5835342, essv5574451, essv6091235, essv5916002, essv5866112, essv5455504, essv5581147, essv6144520, essv5696109, essv5468499, essv6368754, essv5495335, essv6567035, essv6239124, essv5432025, essv6580892, essv5670576, essv5520022, essv6222869, essv5531478 | Samples | NA18577, NA18620, HG01516, HG00403, NA20588, NA12383, NA20761, NA12717, NA11830, HG01173, NA12842, NA20543, NA19664, NA11995, HG00242, NA19204, NA10851, NA12843, NA11920, NA20531, NA11933, NA20816, NA12751, HG00103, NA12004, NA20332, NA18870, NA20771, NA12750, NA12399, NA07357, NA20806, NA18988, HG00271, NA18563, HG01250, NA20796, NA20798, NA19448, HG01177, HG01168, NA12891, NA11992, HG00346, NA12287, HG00369, NA20513, HG00311, NA20541, NA12761, NA20759, HG00277, NA19651, HG01080, HG01067, NA20819, NA06984, HG01519, HG00236, NA20812, HG00262, NA12889, HG00309, NA12828, NA20515, HG00739, HG00264, NA12748, NA11993, HG00108, HG00260, NA20818, NA18614, NA11831, HG00133, HG00380, NA20787, NA12342, NA12878, NA20521, NA20536, NA19663, HG00344, NA19081, HG00275, NA20506, NA20519, HG01149, NA19776, NA20525, HG00284, NA19655, HG00373, NA20581, NA12829, NA11893, NA12249, NA12892, NA06989, HG00117, HG01101, NA12827, NA18963, NA19682, NA19225, NA12778, HG00126, NA18634, NA12546, NA19675, NA20765, NA18546, NA18953, HG00476, NA20773, NA19440, HG01190, HG00265, NA19834, NA12775, HG00366, NA20520, NA20785, NA12046, NA20792, NA19679, NA20544, HG00116, NA20797, HG00256, NA12347, NA19818, NA18971, HG00267, HG01055, NA20510, NA18636, NA20807, NA19116, NA20826, HG00343, NA20528, NA19900, NA20503, NA07056, NA11892, HG01082, HG01125, NA12890, NA07000, NA12154, NA19065 | Known Genes | ADAMTS14 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2662723
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 152 | Observed Complex | 0 | Frequency | n/a |
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