Variant DetailsVariant: nssv2878757Internal ID | 15443650 | Landmark | | Location Information | | Cytoband | 2q37.1 | Allele length | Assembly | Allele length | hg38 | 8769 | hg19 | 8769 | hg18 | 8769 |
| Variant Type | CNV loss | Copy Number | 1 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv514125 | Supporting Variants | | Samples | NA21438 | Known Genes | DNAJB3, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nssv2878757
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|