Variant DetailsVariant: esv2666027 | Internal ID | 9585446 | | Landmark | | | Location Information | | | Cytoband | 9q31.3 | | Allele length | | Assembly | Allele length | | hg38 | 4064 | | hg19 | 4064 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv5888649, essv5527991, essv6467983, essv6398351, essv6350466, essv5784984, essv5993325, essv6392587, essv5464484, essv6536494, essv6539749, essv5845544, essv6049800, essv6130756, essv6117383, essv5641732, essv5562257, essv5998948, essv6567926, essv5642918, essv5411780, essv5815211, essv5438076, essv5427753, essv6501640, essv6217288, essv5758969, essv5653556, essv5484334, essv5451216, essv6196897, essv5936025, essv5648262, essv6530236, essv6401568, essv6335399, essv5682259, essv5558633, essv5735034, essv6061586, essv5946403, essv6002676, essv5767228, essv6469976, essv5943786, essv5479434, essv6545982, essv5437659, essv6189171, essv5726688, essv6331462, essv5587636, essv5426141, essv5821418, essv5847063, essv5781223, essv6408022, essv5811246, essv5495236, essv5926722, essv6532660, essv6105857, essv5726347, essv6370101, essv5845045, essv5963804, essv6043806, essv6566504, essv6457651, essv6379510, essv5530616, essv6131445, essv6008885, essv5879024, essv5592015, essv6386447, essv6022068, essv5471839, essv6587660, essv6397258, essv6186215, essv6366331, essv5547973, essv6096837, essv5490785, essv6260642, essv5590593, essv5409516, essv6207096, essv5697854, essv6387572, essv5913714, essv6419212, essv6310395, essv6293498, essv5570736, essv5727480, essv6434054, essv6107731, essv6512152, essv6428832, essv5869928, essv5721077, essv5586017, essv6371904, essv6431254, essv5723885, essv5670514, essv6186941, essv5934902, essv5574213, essv6472512, essv6539932, essv5948485, essv5651749, essv5915096, essv6544699, essv5604663, essv5972429, essv5452836, essv6180917, essv6364140, essv6301171, essv5564762 | | Samples | HG00403, NA19701, HG00442, NA19058, HG00592, NA19703, HG00536, HG00524, NA19399, NA19332, HG01188, NA19350, NA19359, NA19355, NA18504, NA19377, HG00449, NA19190, NA19067, NA18602, NA19446, NA19374, NA18944, NA18940, NA18550, NA18519, NA19448, NA18595, NA18923, NA19916, NA18558, NA18547, NA19131, NA18942, HG00610, NA19457, NA18571, HG00247, NA19138, NA19384, NA18964, NA19130, HG00512, NA19383, NA19372, NA19385, NA19471, NA19901, NA19209, NA20757, NA20127, NA18867, NA18539, NA18638, NA20818, NA18605, NA19908, NA18613, NA19437, HG00443, NA19056, HG01384, HG00557, NA19152, HG00653, NA19455, NA19236, NA18579, NA18910, NA18630, HG00635, NA18907, NA18573, NA19449, NA19084, HG00531, HG00479, HG00684, HG00613, NA19338, NA19257, HG00704, NA19225, NA19469, NA19160, NA18536, NA19395, NA18570, NA18593, NA18541, NA19436, NA19375, NA18533, NA18909, NA19256, NA19434, NA19473, HG00607, NA19360, HG00662, NA18610, NA19376, NA19398, NA18501, HG00707, HG00578, HG00446, NA19472, NA19713, NA19474, NA19093, NA19102, NA19080, NA20826, NA19430, NA18505, NA18623, NA18612, NA20754, NA19429, NA19346, NA18622, NA18562, HG00581 | | Known Genes | KIAA0368 | | Method | Merging | | Analysis | No reference, merging analysis | | Platform | Merging | | Comments | High quality site | | Reference | 1000_Genomes_Consortium_Phase_1 | | Pubmed ID | 23128226 | | Accession Number(s) | esv2666027
| | Frequency | | Sample Size | 1151 | | Observed Gain | 0 | | Observed Loss | 124 | | Observed Complex | 0 | | Frequency | n/a |
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