Variant DetailsVariant: nsv469687Internal ID | 15187716 | Landmark | | Location Information | | Cytoband | 7q22.1 | Allele length | Assembly | Allele length | hg38 | 182599 | hg19 | 182599 | hg18 | 182599 | hg16 | 182599 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1673118, nssv1672791, nssv1673883, nssv1673585 | Samples | | Known Genes | AP4M1, AZGP1, AZGP1P1, C7orf43, CNPY4, COPS6, LAMTOR4, MBLAC1, MCM7, MIR106B, MIR25, MIR4658, MIR93, TAF6, ZKSCAN1, ZNF3, ZSCAN21 | 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) | nsv469687
| Frequency | Sample Size | 265 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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