View CNVs/SVs
View by Evidence Type: Significant Enriched CNVs (
CNVs Only Present In Patients
de novo CNVs
Overlapping/Recurrent CNVs
CNVs Overlapping With ACRD
CNVs Not Present In Control
Significant Enriched CNVs
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View by Chromosome:8 ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y All )
Notes: ACRD: Autism Chromosome Rearrangement Database
| CNV Name | Chr | Band | Gain/Loss | Number of CNVs | Evidence Type | Reference | |
|---|---|---|---|---|---|---|---|
| Case | Control | ||||||
| AutCNV0000388 | 8 | 8p23.1 | loss | 12 | 8 | Overlapping/Recurrent CNVs; Significant Enriched CNVs; | Cho, 2009 |
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