Variant DetailsVariant: essv5797102Internal ID | 8774505 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 87638 | hg19 | 87638 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | 1 | Merged Status | S | Merged Variants | esv2671474 | Supporting Variants | | Samples | NA18616 | Known Genes | C2CD4C, ODF3L2, SHC2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | essv5797102
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|