Variant DetailsVariant: esv2676630Internal ID | 9596049 | Landmark | | Location Information | | Cytoband | 16p13.3 | Allele length | Assembly | Allele length | hg38 | 3812 | hg19 | 3812 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6159819, essv6498403, essv5536480, essv6435097, essv6111953, essv5600299, essv5972136, essv5646057, essv5677417, essv6336336, essv5862826 | Samples | NA18947, NA18504, NA19190, NA19138, NA19137, NA19238, NA18520, NA19152, NA18909, NA19102, NA18511 | Known Genes | HBA1, HBA2 | 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) | esv2676630
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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