Variant DetailsVariant: nsv515150Internal ID | 15466784 | Landmark | | Location Information | | Cytoband | 9q21.11 | Allele length | Assembly | Allele length | hg38 | 21849 | hg19 | 21849 | hg18 | 21849 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2975400, nssv2975393, nssv2975407, nssv2975395, nssv2975399, nssv2975394, nssv2975396, nssv2975392, nssv2975401, nssv2975404, nssv2975398, nssv2975403, nssv2975405, nssv2975406, nssv2975397, nssv2975402 | Samples | NA21524, NA18862, NA21648, NA12248, NA21635, NA12155, NA21526, NA11994, NA21525, NA19235, NA10831, NA18910, NA18953, NA18952, NA18863, NA19140 | Known Genes | APBA1 | Method | Oligo aCGH | Analysis | ADM2 threshold = 5 | Platform | Agilent Eichler Human CNP 180K v3.0 | Comments | | Reference | Campbell_et_al_2011 | Pubmed ID | 21397061 | Accession Number(s) | nsv515150
| Frequency | Sample Size | 2366 | Observed Gain | 8 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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