Variant DetailsVariant: esv3642965Internal ID | 6683045 | Landmark | | Location Information | | Cytoband | 18q22.2 | Allele length | Assembly | Allele length | hg38 | 16347 | hg19 | 16347 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15927374, essv15927375, essv15927378, essv15927377, essv15927373, essv15927376 | Samples | NA06984, HG03061, HG02775, HG03684, HG03922, HG04056 | Known Genes | DOK6 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3642965
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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