Internal ID | 6676020 |
Landmark | |
Location Information | |
Cytoband | 15q11.2 |
Allele length | Assembly | Allele length | hg38 | 7837 | hg19 | 7837 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | essv15185095, essv15185096, essv15185097, essv15185094 |
Samples | NA18962, NA19005, NA19000, NA19083 |
Known Genes | SNRPN |
Method | Sequencing |
Analysis | |
Platform | Multiple platforms |
Comments | |
Reference | 1000_Genomes_Consortium_Phase_3 |
Pubmed ID | 21293372 |
Accession Number(s) | esv3635910
|
Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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