Variant DetailsVariant: dgv958e199Internal ID | 20124260 | Landmark | | Location Information | | Cytoband | 4q21.1 | Allele length | Assembly | Allele length | hg38 | 2120 | hg19 | 2120 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2665048, esv2671343 | Samples | NA18628 | Known Genes | SCARB2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | dgv958e199
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|