Variant DetailsVariant: nsv514550Internal ID | 15466186 | Landmark | | Location Information | | Cytoband | 10p11.23 | Allele length | Assembly | Allele length | hg38 | 4349 | hg19 | 4349 | hg18 | 4349 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2777455, nssv2772409, nssv2773144, nssv2774742, nssv2769047, nssv2769198, nssv2768951, nssv2769425, nssv2771266 | Samples | NA18489, NA19151, NA18856, NA18857, NA19094, NA19108, NA19149, NA19109, NA19093 | Known Genes | MPP7 | 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) | nsv514550
| Frequency | Sample Size | 2366 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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