Variant DetailsVariant: essv13628652Internal ID | 3630468 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 184120 | hg19 | 184120 |
| Variant Type | CNV loss | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3621839 | Supporting Variants | | Samples | HG03861 | Known Genes | C9orf78, MIR6855, PRRX2, PTGES, TOR1A, TOR1B, USP20 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv13628652
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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