Variant DetailsVariant: nsv8697Internal ID | 15499923 | Landmark | | Location Information | | Cytoband | 10q22.3 | Allele length | Assembly | Allele length | hg38 | 36028 | hg19 | 36028 | hg18 | 36028 | hg17 | 36028 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv17599, nssv18534, nssv20198, nssv19727, nssv24405, nssv22403, nssv19324, nssv19066 | Samples | NA12155, NA18563, NA10839, NA18975, NA18572, NA19221, NA18972, NA18552 | Known Genes | NUTM2B | 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) | nsv8697
| Frequency | Sample Size | 31 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
|
|