Variant DetailsVariant: essv16173466Internal ID | 6175282 | Landmark | | Location Information | | Cytoband | 20q11.21 | Allele length | Assembly | Allele length | hg38 | 75855 | hg19 | 75855 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3645652 | Supporting Variants | | Samples | HG00759 | Known Genes | HM13, HM13-AS1, PSIMCT-1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv16173466
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|