Variant DetailsVariant: nsv1020397Internal ID | 18762932 | Landmark | | Location Information | | Cytoband | 5q13.3 | Allele length | Assembly | Allele length | hg38 | 42447 | hg19 | 42447 | hg18 | 42447 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv5703n100 | Supporting Variants | nssv3639034, nssv3639032, nssv3639027, nssv3639035, nssv3639026, nssv3639028, nssv3639031, nssv3747326, nssv3639033, nssv3747325, nssv3639029, nssv3639036, nssv3747327, nssv3639030, nssv3747324 | Samples | | Known Genes | F2RL1 | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | nsv1020397
| Frequency | Sample Size | 29084 | Observed Gain | 15 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|