Variant DetailsVariant: nsv8761Internal ID | 15499987 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 4654 | hg19 | 4654 | hg18 | 4654 | hg17 | 4654 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv17680, nssv19725, nssv19653, nssv22244, nssv18692, nssv20109, nssv21703 | Samples | NA07029, NA18504, NA12802, NA07048, NA18537, NA18517, NA12740 | Known Genes | AP2A2 | 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) | nsv8761
| Frequency | Sample Size | 31 | Observed Gain | 7 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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