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 | essv5845544, essv6408022, essv6398351, essv5847063, essv6301171, essv6310395, essv5972429, essv6130756, essv6293498, essv6131445, essv5811246, essv6567926, essv5471839, essv5527991, essv5670514, essv6189171, essv5879024, essv5530616, essv5586017, essv5845045, essv5936025, essv6217288, essv6539932, essv5993325, essv5815211, essv6331462, essv5641732, essv5963804, essv6469976, essv5437659, essv6472512, essv5888649, essv6392587, essv6401568, essv5562257, essv6008885, essv6366331, essv6350466, essv5697854, essv5721077, essv6061586, essv6196897, essv5409516, essv5558633, essv5682259, essv5490785, essv5926722, essv6539749, essv6022068, essv5464484, essv5426141, essv6419212, essv5452836, essv5735034, essv5648262, essv6049800, essv6397258, essv6002676, essv5998948, essv5427753, essv5479434, essv6260642, essv5642918, essv5451216, essv5784984, essv6566504, essv6117383, essv5495236, essv6431254, essv5758969, essv5570736, essv6105857, essv6335399, essv5574213, essv5943786, essv6457651, essv5587636, essv6207096, essv6587660, essv6379510, essv6530236, essv5934902, essv6532660, essv6536494, essv6186941, essv5726688, essv6096837, essv6545982, essv5727480, essv6434054, essv5946403, essv5547973, essv5564762, essv5821418, essv5484334, essv5651749, essv6107731, essv6467983, essv6387572, essv5869928, essv6186215, essv5653556, essv5726347, essv6428832, essv6544699, essv5781223, essv6180917, essv6512152, essv6386447, essv5767228, essv6364140, essv5590593, essv5604663, essv5913714, essv5411780, essv5948485, essv5723885, essv6371904, essv5915096, essv5438076, essv6043806, essv5592015, essv6501640, essv6370101 | Samples | HG00613, NA18964, NA19152, NA19436, NA18605, HG00536, HG00607, NA18595, NA18630, NA19437, NA18612, NA19209, NA18501, NA19093, HG00449, NA19469, NA18550, NA18570, HG00707, NA19455, NA19430, NA19359, NA19338, NA19449, NA18573, HG00446, NA18541, HG01188, HG00581, HG00557, NA19257, HG00578, NA19701, NA19236, NA19355, NA19474, NA19084, NA18505, NA19472, HG00479, HG00247, HG00592, HG00635, NA19067, NA19383, HG01384, NA18536, NA18622, NA18623, NA19471, NA20757, HG00610, NA20754, NA20127, NA18638, NA19398, NA19429, NA19908, NA18547, NA19256, NA18593, NA19056, HG00403, NA19457, HG00662, NA18539, NA19190, NA19360, NA19377, NA19395, NA19080, NA19372, HG00653, NA19374, NA19703, NA19375, NA19384, NA18923, NA20826, NA19102, NA19713, NA18558, NA19901, NA18504, NA20818, NA18942, NA19332, NA18613, HG00524, HG00512, NA18562, NA19131, NA18910, NA18579, NA18940, NA19138, NA19376, HG00443, NA18907, NA18909, NA18867, NA19434, NA18602, NA19446, NA18533, NA18944, NA19225, NA19399, NA19160, NA18571, NA19916, NA18610, NA19130, NA19346, HG00442, NA19350, NA19473, HG00684, NA19448, HG00704, NA19385, NA18519, NA19058, HG00531 | 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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