Variant DetailsVariant: essv14669655Internal ID | 4671471 | Landmark | | Location Information | | Cytoband | 13q12.12 | Allele length | Assembly | Allele length | hg38 | 131837 | hg19 | 131837 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3631523 | Supporting Variants | | Samples | HG03571 | Known Genes | LINC00327, TNFRSF19 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv14669655
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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