Extended Data Table 1 CNVs hitting TADA genes
From: Synaptic, transcriptional and chromatin genes disrupted in autism
- Count of deletion CNVs inferred from sequence for ASD subjects and those unaffected by ASD. Number of subjects and family status: 849 ASD subjects without family information; 1,467 ASD subjects in families; 2,766 unaffected parents; 319 unaffected siblings of ASD subjects; 373 unaffected subjects without family information. NT, parent a carrier but CNV not transmitted to affected child; Tr-ASD, transmitted to ASD subject from carrier parent; Tr-not-ASD, parent transmits a CNV to an unaffected child.
- *No parents in this count were affected; seven parents in the study were affected, none carried a CNV reported in the table and these subjects did not enter the calculation.
- †To compute the odds ratio we count the number of affected carriers (a), unaffected carriers (including parents) (b), affected subjects who do not have the CNV (c), and unaffected non-carriers (d). The odds ratio = (ad)/(bc).
- ‡One parent transmits the CNV to an affected and unaffected offspring; to obtain the total count of controls with a CNV, subtract one.
- §Genes are adjacent in the genome (see Extended Data Fig. 4). For three subjects both genes are affected by the same CNV (1 ASD and 2 unaffected subjects).