Variant DetailsVariant: esv3639301| Internal ID | 6679396 | | Landmark | | | Location Information | | | Cytoband | 16q23.2 | | Allele length | | Assembly | Allele length | | hg38 | 46048 | | hg19 | 46048 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv544e214 | | Supporting Variants | essv15535536, essv15535531, essv15535535, essv15535534, essv15535530, essv15535532, essv15535533, essv15535537 | | Samples | HG03455, HG00335, NA19471, NA19037, NA19331, NA19334, HG03157, NA19351 | | Known Genes | | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3639301
| | Frequency | | Sample Size | 2504 | | Observed Gain | 0 | | Observed Loss | 8 | | Observed Complex | 0 | | Frequency | n/a |
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