T19. DECOMPOSING PHENOTYPIC DISPERSION IN 16P11.2 COPY NUMBER VARIATION ACROSS TRAITS AND INDIVIDUALS
Background Rare recurrent copy number variants (CNVs) are associated with risk for developmental and neuropsychiatric disorders but demonstrate considerable clinical heterogeneity at the individual level. It remains unclear how between-person variability within CNV groups compares to the general population, differs acr...
Tyler Dietterich, Rune Bøen, Hoki Fung et al.
· European Neuropsychopharmaco... · 0 citations