Variant DetailsVariant: nsv8298Internal ID | 15499524 | Landmark | | Location Information | | Cytoband | 8p22 | Allele length | Assembly | Allele length | hg38 | 1033837 | hg19 | 1033837 | hg18 | 1033837 | hg17 | 1033837 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv15491, nssv17496, nssv19913, nssv18128, nssv16954, nssv19377, nssv20970, nssv19347, nssv19401 | Samples | NA12155, NA18860, NA10839, NA10863, NA12872, NA19221, NA19132, NA18972 | Known Genes | MIR383, SGCZ, TUSC3 | 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) | nsv8298
| Frequency | Sample Size | 31 | Observed Gain | 2 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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