Variant DetailsVariant: nsv9446Internal ID | 15500672 | Landmark | | Location Information | | Cytoband | 16q12.2 | Allele length | Assembly | Allele length | hg38 | 26885 | hg19 | 26885 | hg18 | 26885 | hg17 | 26885 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv20569, nssv23185, nssv26620, nssv23326, nssv24988, nssv23089, nssv23800, nssv21652, nssv23596, nssv23729 | Samples | NA18980, NA12155, NA18563, NA18942, NA07048, NA10839, NA18572, NA18537, NA18517, NA18564 | Known Genes | CES1 | Method | Oligo aCGH | Analysis | Statistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2 | Platform | Agilent-015686 Custom Human 244K CGH Microarray | Comments | | Reference | Perry_et_al_2008 | Pubmed ID | 18304495 | Accession Number(s) | nsv9446
| Frequency | Sample Size | 31 | Observed Gain | 10 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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