Variant DetailsVariant: nsv469537Internal ID | 15187566 | Landmark | | Location Information | | Cytoband | 17q21.31 | Allele length | Assembly | Allele length | hg38 | 161242 | hg19 | 161242 | hg18 | 161182 | hg16 | 161182 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1674426, nssv1673495, nssv1673822, nssv1675196, nssv1673032 | Samples | | Known Genes | KANSL1, MAPT | 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) | nsv469537
| Frequency | Sample Size | 265 | Observed Gain | 1 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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