Variant DetailsVariant: nsv469891Internal ID | 15187920 | Landmark | | Location Information | | Cytoband | 17p13.3 | Allele length | Assembly | Allele length | hg38 | 174132 | hg19 | 174132 | hg18 | 174132 | hg16 | 174132 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1672439 | Samples | | Known Genes | DBIL5P, FAM57A, GEMIN4, GLOD4, NXN, RNMTL1, VPS53 | 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) | nsv469891
| Frequency | Sample Size | 265 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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