Variant DetailsVariant: essv12786795Internal ID | 2788611 | Landmark | | Location Information | | Cytoband | 7p11.2 | Allele length | Assembly | Allele length | hg38 | 155750 | hg19 | 155750 |
| Variant Type | CNV gain | Copy Number | | Allele State | Heterozygous | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv3613258 | Supporting Variants | | Samples | NA12828 | Known Genes | CCT6A, CHCHD2, GBAS, NUPR1L, PHKG1, PSPH, SNORA15, SUMF2 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | essv12786795
| Frequency | Sample Size | 2504 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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