Internal ID | 15504176 |
Landmark | |
Location Information | |
Cytoband | 10q11.22 |
Allele length | Assembly | Allele length | hg38 | 49445 | hg19 | 50819 | hg18 | 50819 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nssv626049 |
Samples | 1 |
Known Genes | LINC00842, LOC100996758, NPY4R |
Method | SNP array |
Analysis | Analysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array |
Platform | GPL8882 |
Comments | |
Reference | Arlt_et_al_2011 |
Pubmed ID | 21212237 |
Accession Number(s) | nsv511437
|
Frequency | Sample Size | 1 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|