Variant DetailsVariant: esv3891984Internal ID | 18839694 | Landmark | | Location Information | | Cytoband | 11p11.12 | Allele length | Assembly | Allele length | hg38 | 657407 | hg19 | 657407 | hg18 | 657407 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25791893, essv25790937 | Samples | | Known Genes | FOLH1, TRIM49B, TRIM64C | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891984
| Frequency | Sample Size | 3017 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|