Variant DetailsVariant: esv2668102 Internal ID | 9587521 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 148 | hg19 | 148 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6581011, essv5705934, essv6392861, essv5588882, essv6315663, essv6329733, essv6571385, essv5945143, essv5926180, essv6556420, essv6531823, essv5571208, essv6471245, essv5892795, essv5582063, essv6009976, essv6106535, essv6548821, essv6321791, essv5734290, essv5486853, essv6297149, essv5522549, essv5582435, essv5903053, essv6071843, essv5546520, essv6264203, essv6150163, essv6350790, essv6391070, essv6400593, essv6215800, essv6528811, essv6264382, essv5638261, essv5890471, essv6473394, essv6573755, essv5822932, essv6572637, essv5523516, essv5931724, essv6162116, essv5760015, essv5553604, essv5788544, essv5492541, essv6100674, essv5937138, essv5439296, essv5847066, essv5412631, essv5954309, essv5655124, essv6078967, essv6450839, essv5779249, essv6244565, essv5721912, essv6239042, essv5463742, essv6045543, essv5460220, essv5729344, essv6213726, essv6143451, essv5747931, essv6469269, essv5441003, essv6551003, essv6180999, essv6520334, essv6268367 | Samples | HG00671, NA19066, HG00524, NA18561, NA18999, NA18603, NA19057, NA18530, NA18988, NA19068, NA18944, NA18550, HG01070, HG00589, HG00501, HG01177, HG01488, NA18567, HG00330, NA18547, NA18960, NA18618, NA19054, NA18964, HG00537, NA19079, NA18611, HG00512, HG01069, HG00325, HG00422, NA18986, NA18557, NA18985, HG00313, NA18544, HG00657, HG00584, NA18572, NA18534, HG00708, HG00531, HG00684, HG00613, HG00525, NA18553, NA18555, HG00704, NA18634, NA18541, NA19012, NA18576, NA18546, NA18608, NA19685, NA18953, NA18543, HG00625, NA18628, HG00580, HG00607, NA18943, HG00418, HG00672, HG00513, NA18552, NA18984, NA18989, NA19063, NA19065, NA18612, NA18549, HG01061, NA18577 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2668102
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 74 | Observed Complex | 0 | Frequency | n/a |
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