Variant DetailsVariant: esv3631536Internal ID | 6671662 | Landmark | | Location Information | | Cytoband | 13q12.12 | Allele length | Assembly | Allele length | hg38 | 120904 | hg19 | 120904 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv14669733 | Samples | HG03571 | Known Genes | ANKRD20A19P, C1QTNF9B, C1QTNF9B-AS1, MIPEP, SPATA13 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3631536
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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