Variant DetailsVariant: nsv469559Internal ID | 15187588 | Landmark | | Location Information | | Cytoband | 11q12.1 | Allele length | Assembly | Allele length | hg38 | 156855 | hg19 | 156855 | hg18 | 156855 | hg16 | 156855 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1675470, nssv1675620 | Samples | | Known Genes | FAM111B, LOC283194 | Method | BAC aCGH | Analysis | A locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments. | Platform | GPL4010 | Comments | | Reference | Locke_et_al_2006 | Pubmed ID | 16826518 | Accession Number(s) | nsv469559
| Frequency | Sample Size | 265 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|