Variant DetailsVariant: nssv2762673Internal ID | 17509927 | Landmark | | Location Information | | Cytoband | 1p22.3 | Allele length | Assembly | Allele length | hg38 | 259221 | hg19 | 259221 | hg18 | 259221 |
| Variant Type | CNV duplication | Copy Number | 3 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv947434 | Supporting Variants | | Samples | HGDP01029 | Known Genes | LPAR3, MCOLN2, MCOLN3, WDR63 | Method | Sequencing | Analysis | Human CNVs | Platform | Not reported | Comments | | Reference | Sudmant_et_al_2013 | Pubmed ID | 23825009 | Accession Number(s) | nssv2762673
| Frequency | Sample Size | 10 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|