Variant DetailsVariant: nsv8859Internal ID | 15500085 | Landmark | | Location Information | | Cytoband | 11q14.3 | Allele length | Assembly | Allele length | hg38 | 55137 | hg19 | 55137 | hg18 | 55137 | hg17 | 55137 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv23529, nssv23251, nssv18190, nssv20859, nssv20597, nssv20475 | Samples | NA18563, NA12802, NA18537, NA19132, NA12740, NA18972 | Known Genes | UBTFL1 | 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) | nsv8859
| Frequency | Sample Size | 31 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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