Variant DetailsVariant: nsv469547 Internal ID | 15187576 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 163251 | hg19 | 163251 | hg18 | 163251 | hg16 | 163251 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1674519, nssv1673720, nssv1673217, nssv1675743, nssv1674292, nssv1676381, nssv1674138, nssv1672405, nssv1674723, nssv1675151, nssv1672752, nssv1675539, nssv1673745, nssv1676112, nssv1674844, nssv1675970, nssv1674155, nssv1675234, nssv1673613, nssv1672159, nssv1675588, nssv1674424, nssv1675742, nssv1672716, nssv1672674, nssv1676220, nssv1674291, nssv1672424, nssv1674204, nssv1673832, nssv1672535, nssv1674776, nssv1674672, nssv1672880 | Samples | | Known Genes | GOLGA8A, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, SLC12A6 | 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) | nsv469547
| Frequency | Sample Size | 265 | Observed Gain | 0 | Observed Loss | 34 | Observed Complex | 0 | Frequency | n/a |
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