Variant DetailsVariant: esv2663963 Internal ID | 9583382 | Landmark | | Location Information | | Cytoband | 2p23.3 | Allele length | Assembly | Allele length | hg38 | 333 | hg19 | 333 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5792770, essv6247855, essv5647242, essv5429664, essv6053057, essv5828597, essv6368419, essv6303370, essv5679601, essv6592455, essv6288808, essv6498284, essv5970372, essv6285050, essv5533947, essv6472302, essv5784675, essv6003552, essv5821568, essv5914283, essv5417385, essv5673435, essv5874503, essv5814596, essv5897860, essv5771487, essv6151875, essv6269747, essv6080073, essv5756258, essv5731103, essv6006995, essv6181617, essv5845056, essv6502504, essv6495533, essv5921882, essv6335090, essv6256555, essv5601913, essv5976571, essv6433673, essv6219988, essv6206374, essv6356310, essv6414960, essv5887590, essv6422590, essv6161561, essv5433077, essv5546927, essv6318753, essv5626283, essv6566962, essv5405506, essv5437048, essv6078954, essv6387508, essv5511292, essv6216699, essv6561001, essv6213766, essv6292075, essv5927716, essv5463054, essv5820590, essv6573025, essv5504202, essv5550269, essv5724127, essv6186645, essv6366251, essv5850204, essv6050315, essv6276060, essv5729803, essv5977186, essv5891594, essv6157313, essv5453292, essv6179406, essv5532642, essv6586231, essv5983595, essv5892971, essv5905068, essv6049061, essv6152746, essv5408882, essv5883556, essv5857349, essv6156900, essv6323173, essv5601220, essv6062039, essv5703304, essv5491776, essv6195712, essv6076917, essv5868452, essv5615170, essv5596270, essv6542006, essv6282631, essv6518029, essv5422057, essv5859788, essv5539207, essv5827666, essv5562248, essv5540575, essv5981247 | Samples | NA19701, HG01173, NA19700, HG01521, HG00143, NA19703, HG00142, HG00249, NA19399, NA19704, HG01374, NA19350, NA12004, NA19684, NA19377, NA12058, HG00737, HG00150, HG01461, NA19443, NA19920, NA12399, HG01140, NA19381, NA19379, NA18519, NA19315, HG01177, HG01488, NA20774, NA19198, NA19197, NA20768, NA19313, HG00369, NA20287, HG00243, HG00139, HG01069, HG01080, NA20278, HG00148, NA06984, NA20340, NA19372, HG01440, NA19722, NA19901, HG00338, HG00326, HG00253, NA18539, NA19921, NA19451, HG01353, HG00137, HG00133, HG01136, HG00188, NA19908, NA12342, NA12003, HG01095, HG00368, NA19236, NA19982, HG00275, NA20519, HG01073, NA19461, HG01197, HG01383, HG00157, HG01334, NA18523, NA19469, NA20534, HG01204, HG01075, HG01148, NA19401, NA19375, NA20522, NA20801, HG00336, NA19712, NA19747, NA19435, HG00638, NA19331, HG00308, NA19334, NA20778, NA19428, NA19311, NA19360, HG00256, NA12347, HG00269, NA19328, HG00259, NA19472, HG00342, NA20334, HG01055, NA19116, HG00343, HG00372, NA19129, HG01125, NA20322, NA19429 | Known Genes | CIB4 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2663963
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 112 | Observed Complex | 0 | Frequency | n/a |
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