Variant DetailsVariant: esv2724073 Internal ID | 9958374 | Landmark | | Location Information | | Cytoband | 1q42.13 | Allele length | Assembly | Allele length | hg38 | 669 | hg19 | 669 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6675384, essv6895986, essv6847307, essv6692962, essv6777106, essv6933490, essv6968120, essv6720198, essv6773618, essv6955027, essv6859410, essv6886122, essv6729795, essv6961830, essv6937853, essv6738986, essv6753651, essv6769704, essv6810471, essv6759200, essv6785173, essv6781060, essv6836354, essv6898759, essv6832748, essv6789340, essv6697122, essv6917620, essv6840133 | Samples | SSM100, SSM083, SSM027, SSM065, SSM038, SSM088, SSM058, SSM028, SSM084, SSM021, SSM047, SSM069, SSM061, SSM096, SSM026, SSM017, SSM032, SSM067, SSM086, SSM066, SSM068, SSM082, SSM007, SSM037, SSM076, SSM022, SSM070, SSM099, SSM052 | Known Genes | ADCK3 | 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) | esv2724073
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
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