Variant DetailsVariant: nsv10442 Internal ID | 15498719 | Landmark | | Location Information | | Cytoband | 4p16.1 | Allele length | Assembly | Allele length | hg38 | 19802 | hg19 | 19801 | hg18 | 19801 | hg17 | 19801 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv12091, nssv12123, nssv11747, nssv11522, nssv11750, nssv12591, nssv11737, nssv13800, nssv11496, nssv29162, nssv12732, nssv28837, nssv13613, nssv11626, nssv11758, nssv12938, nssv29048, nssv12807, nssv12359, nssv12189, nssv12034, nssv12078, nssv12024, nssv11755 | Samples | NA18502, NA11830, NA18980, NA07029, NA12155, NA18563, NA12802, NA18860, NA07048, NA10839, NA18975, NA10847, NA10863, NA12872, NA19221, NA18853, NA19132, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552 | Known Genes | CPZ | 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) | nsv10442
| Frequency | Sample Size | 31 | Observed Gain | 24 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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