Variant DetailsVariant: nsv9290Internal ID | 15500516 | Landmark | | Location Information | | Cytoband | 15q25.2 | Allele length | Assembly | Allele length | hg38 | 403291 | hg19 | 277770 | hg18 | 287770 | hg17 | 287770 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv25422, nssv27578, nssv23122, nssv26349, nssv22246, nssv24802, nssv27570, nssv22615, nssv25916, nssv26076 | Samples | NA18502, NA18980, NA18860, NA19221, NA19132, NA18517, NA19240, NA12740, NA18552 | Known Genes | DNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1 | 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) | nsv9290
| Frequency | Sample Size | 31 | Observed Gain | 3 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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