Variant DetailsVariant: esv2660354 Internal ID | 9579773 | Landmark | | Location Information | | Cytoband | 21q21.3 | Allele length | Assembly | Allele length | hg38 | 199 | hg19 | 199 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5653988, essv6040978, essv5649477, essv5594185, essv5743123, essv5953251, essv5650571, essv6481927, essv6055640, essv5706888, essv6054382, essv6365583, essv5776692, essv6284323, essv5404260, essv6069853, essv5622234, essv5597431, essv6168123, essv6035278, essv6360763, essv5480239, essv6021009, essv5798881, essv6563739, essv6570537, essv6028009, essv6289941, essv6353232, essv6136539, essv6051873, essv6557295, essv6164699, essv6550977, essv6445461, essv5717438, essv6563148, essv5716667, essv6007849, essv6148450, essv6192768, essv6425159, essv5619845, essv6035150, essv6293493, essv5887933, essv6591006, essv5801069, essv6473779, essv5475459, essv5825240, essv5934878, essv5771937, essv5710581, essv5802560, essv6433737, essv6352582, essv6439319, essv5994916, essv6508347, essv6328234, essv5921996, essv5952344, essv6182522, essv6032425, essv5513952, essv5982591, essv5913906, essv6498582, essv5623741, essv5715497 | Samples | HG01441, HG01356, HG00536, HG00608, HG00671, NA18603, HG00699, NA18545, NA18959, HG00654, NA18526, NA18563, NA18550, NA18597, HG00702, HG00689, NA18635, NA18558, NA18547, HG01083, HG00537, NA18949, NA18611, NA19731, HG00422, HG00705, HG01440, NA18557, NA18973, HG00530, NA18638, HG00543, NA18951, NA18613, NA19657, HG01384, HG00557, NA18956, HG00701, NA19663, NA18637, NA18579, NA18948, HG00708, HG00692, NA18573, HG00651, HG00690, HG00531, HG00684, HG00525, NA18555, HG00463, NA18536, HG01107, NA18546, NA18632, NA18542, HG00353, HG00580, HG00607, NA18943, HG00418, HG00672, HG00614, HG00421, HG00656, NA18609, NA18612, NA18622, NA18562 | Known Genes | APP | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660354
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 71 | Observed Complex | 0 | Frequency | n/a |
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