Variant DetailsVariant: esv3637455| Internal ID | 7024247 | | Landmark | | | Location Information | | | Cytoband | 15q26.3 | | Allele length | | Assembly | Allele length | | hg38 | 89390 | | hg19 | 89390 |
| | Variant Type | CNV gain | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv15346495, essv15346491, essv15346494, essv15346490, essv15346496, essv15346492, essv15346493 | | Samples | NA19028, NA19141, HG02678, NA19834, HG00620, HG04171, NA18488 | | Known Genes | ADAMTS17 | | Method | Sequencing | | Analysis | | | Platform | Multiple platforms | | Comments | | | Reference | 1000_Genomes_Consortium_Phase_3 | | Pubmed ID | 21293372 | | Accession Number(s) | esv3637455
| | Frequency | | Sample Size | 2504 | | Observed Gain | 7 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
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