Variant DetailsVariant: nsv515126Internal ID | 15466760 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 1457 | hg19 | 1457 | hg18 | 1457 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2970571, nssv2970573, nssv2970577, nssv2970579, nssv2970572, nssv2970583, nssv2970574, nssv2970585, nssv2970581, nssv2970570, nssv2970582, nssv2970575, nssv2970584, nssv2970580, nssv2970578, nssv2970576, nssv2970569 | Samples | NA21403, NA21635, NA19127, NA19201, NA19119, NA19138, NA19128, NA18908, NA18910, NA18503, NA19202, NA19108, NA21615, NA18911, NA21404, NA19129, NA19214 | Known Genes | | 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) | nsv515126
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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