Variant DetailsVariant: dgv372n27Internal ID | 20132630 | Landmark | | Location Information | | Cytoband | 17q25.1 | Allele length | Assembly | Allele length | hg38 | 859787 | hg19 | 859787 | hg18 | 859787 | hg17 | 859787 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv457902, nsv457901 | Samples | NINDS_116, NINDS_131 | Known Genes | BTBD17, C17orf77, CD300A, CD300C, CD300E, CD300LB, CD300LD, DNAI2, GPR142, GPRC5C, KIF19, LINC00469, MGC16275, RAB37, RPL38, TTYH2 | Method | SNP array | Analysis | An HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives. | Platform | Not reported | Comments | | Reference | Itsara_et_al_2009 | Pubmed ID | 19166990 | Accession Number(s) | dgv372n27
| Frequency | Sample Size | 1557 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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