Skip to main content
. 2020 Sep 6;30(1):305–318. doi: 10.1002/jgc4.1323

TABLE 2.

Characteristics of the genome to outcome cohort (n = 113)

Characteristic Statistic
Child’s age on study referral in years M (SD) 6.7 (3.71)
Child’s gender N (%)
Male 84 (74.3)
Female 29 (25.7)
Child’s diagnosis N (%)
ASD 97 (85.8)
DD/ID 16 (14.2)
Number of child’s siblings
0 31 (27.4)
1 60 (53.1)
2 or more 22 (19.5)
Caregiver’s age on study visit in years M (SD) 39.3 (7.9)
Caregiver’s relationship to child N (%)
Biological mother 98 (86.7)
Biological father 11 (9.7)
Adoptive mother 4 (3.5)
Marital status N (%)
Married/common law 96 (85.0)
Single/separated/divorced 17 (15.0)
Respondent education background N (%)
High school or College 53 (46.9)
University or post‐secondary 60 (53.1)
Annual household income N (%)
Less than $40,000 34 (30.1)
Between $40,000 and $80,000 35 (30.1)
More than $80,000 43 (38.1)
Missing 1 (0.9)
Referral source N (%)
Pediatrics 66 (58.4)
Medical genetics 18 (15.9)
Psychology 12 (10.6)
Self‐referred 12 (10.6)
Neurology 5 (4.4)
CMA results available prior to referral
Yes 36 (31.9)
No 70 (61.9)
Missing 7 (6.2)
Time between study visit and referral in weeks, median (range) 6.4 (1.0‐68.7)
Time between study referral and final diagnostic report in weeks, median (range) 3.3 (−1‐548)

Abbreviations: ASD, Autism spectrum disorder; CMA, chromosomal microarray imaging; DD/ID, Developmental delay/Intellectual disability; M, Mean; SD, Standard deviation.