Variant DetailsVariant: nsv10409Internal ID | 15498686 | Landmark | | Location Information | | Cytoband | 4p16.3 | Allele length | Assembly | Allele length | hg38 | 61423 | hg19 | 61315 | hg18 | 61315 | hg17 | 61315 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv12612, nssv11677, nssv13620, nssv12501, nssv11707 | Samples | NA18502, NA11830, NA18860, NA19221 | Known Genes | ZNF595, ZNF718 | 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) | nsv10409
| Frequency | Sample Size | 31 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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