Variant DetailsVariant: nsv9712Internal ID | 15500938 | Landmark | | Location Information | | Cytoband | 19q13.12 | Allele length | Assembly | Allele length | hg38 | 15602 | hg19 | 15602 | hg18 | 15602 | hg17 | 15602 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv24330, nssv25121, nssv21910, nssv24765, nssv25102, nssv25096, nssv22000, nssv27498, nssv25520, nssv21605, nssv25027, nssv24790, nssv25046, nssv25497, nssv24332, nssv22061, nssv25077, nssv25071, nssv25419, nssv21970, nssv21940, nssv24161, nssv25052, nssv22121, nssv25474 | Samples | NA18563, NA12802, NA07048, NA18975, NA19007, NA10847, NA10863, NA12872, NA18564, NA12740, NA18972 | Known Genes | FFAR3 | 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) | nsv9712
| Frequency | Sample Size | 31 | Observed Gain | 0 | Observed Loss | 11 | Observed Complex | 0 | Frequency | n/a |
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