Variant DetailsVariant: nsv9477Internal ID | 15500703 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 38765 | hg19 | 38765 | hg18 | 38765 | hg17 | 38765 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv28131, nssv26749, nssv26791, nssv23285, nssv22685, nssv24175, nssv25268, nssv26625, nssv25927, nssv24149, nssv22770, nssv23837, nssv22072 | Samples | NA18502, NA18980, NA07029, NA18504, NA12155, NA18942, NA07048, NA10863, NA19221, NA19132, NA18517, NA12740 | Known Genes | CPNE7 | 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) | nsv9477
| Frequency | Sample Size | 31 | Observed Gain | 11 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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