Variant DetailsVariant: nsv9357Internal ID | 15500583 | Landmark | | Location Information | | Cytoband | 16p13.11 | Allele length | Assembly | Allele length | hg38 | 77891 | hg19 | 77891 | hg18 | 77891 | hg17 | 77891 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv26359, nssv23099, nssv26649, nssv25066, nssv25907, nssv22398, nssv20932, nssv22850, nssv22938, nssv21954, nssv25741 | Samples | NA18502, NA18980, NA18504, NA18860, NA18942, NA18975, NA19007, NA18537, NA18517, NA18564, NA18972 | Known Genes | MIR1972-1, MIR1972-2, PDXDC1 | 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) | nsv9357
| Frequency | Sample Size | 31 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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