Variant DetailsVariant: esv2657167 Internal ID | 9576586 | Landmark | | Location Information | | Cytoband | 1p22.3 | Allele length | Assembly | Allele length | hg38 | 157 | hg19 | 157 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6369036, essv5669557, essv5904158, essv5997429, essv5944962, essv6141134, essv5941848, essv5717916, essv5912079, essv6449223, essv6261292, essv5883364, essv6347556, essv5927908, essv6029897, essv5937689, essv5831353, essv5510722, essv5679548, essv5423180, essv6004440, essv6030565, essv5771695, essv5755320, essv5812776, essv6486775, essv5483860, essv5434742, essv5814412, essv5521779, essv6058453, essv5525644, essv5918673, essv5535295 | Samples | HG00608, NA18947, NA19066, HG00524, NA18486, NA18944, NA18940, HG00689, HG00330, NA18574, NA18571, HG00512, NA18977, NA11994, NA18617, NA19210, HG00596, HG00584, NA18948, NA18537, HG00324, HG00684, HG00613, NA18553, NA18555, HG00704, HG00614, HG00513, HG00478, HG00310, NA18623, NA18549, HG01191, NA18620 | Known Genes | ODF2L | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2657167
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 34 | Observed Complex | 0 | Frequency | n/a |
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