Variant DetailsVariant: esv2729973Internal ID | 9964288 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 775 | hg19 | 775 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6958623, essv6672542, essv6850580, essv6763149, essv6906007, essv6856611, essv6734938, essv6757966, essv6965165, essv6861922, essv6832199, essv6809096, essv6755246, essv6752294 | Samples | SSM059, SSM027, SSM075, SSM087, SSM088, SSM002, SSM057, SSM058, SSM062, SSM026, SSM031, SSM086, SSM010, SSM049 | Known Genes | ADARB2 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2729973
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 14 | Observed Complex | 0 | Frequency | n/a |
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