Variant DetailsVariant: essv15674492Internal ID | 5676308 | Landmark | | Location Information | | Cytoband | 17q21.2 | Allele length | Assembly | Allele length | hg38 | 220979 | hg19 | 220979 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3640559 | Supporting Variants | | Samples | HG03913 | Known Genes | KRT23, KRT39, KRT40, KRTAP1-1, KRTAP1-3, KRTAP1-4, KRTAP1-5, KRTAP2-1, KRTAP2-2, KRTAP2-3, KRTAP2-4, KRTAP3-1, KRTAP3-2, KRTAP3-3, KRTAP4-11, KRTAP4-7, KRTAP4-8, KRTAP4-9 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv15674492
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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