Objective：To investigate the molecular diagnostic value of whole exome sequencing (WES)in the genetic etiology of intellectual disability (ID) or global developmental delay (GDD) and analysis of genetic characteristics in the Chinese cohort. Methods：1096 patients with ID/GDD who were enrolled in Children's Hospital of Nanjing Medical University from January 2019 to December 2021 were selected as the study objects. Inclusion criteria adhered to clinical guidelines for significant developmental milestone delays, with exclusion of non-genetic factors (e. g. , perinatal hypoxia, infection, metabolic abnormalities). We retrospectively analyzed sequence variants and copy number variations (CNVs) detected by Trio- whole exome sequencing (Trio-WES) or proband-only WES, classifying variants according to the American College of Medical Genetics and Genomics (ACMG) guidelines, with pathogenic（P）/likely pathogenic(LP) variants defined as positive results. Results：1096 patients with ID/GDD ranged in age from 1 month to 15 years, with a median age of 24(12, 48) months, including 716 males and 380 females. The overall positive diagnostic rate was 35.31%(387/1096), with monogenic variants identified in 271 patients and CNVs in 116 patients. Among the monogenic variants, MECP2 gene was the most common one（12/271, 4.43%），primarily associated with Rett syndrome, followed by SYNGAP1 and DDX3X. For CNVs, 5.17%（6/116）patients were aneuploidies，with 7q11.23 deletions (associated with Williams syndrome) being most common (8.62%, 10/116). Autosomal dominant inheritance accounted for 71.96% (195/271) of monogenic variants, while X-linked inheritance represented 19.93% (54/271). Sanger sequencing confirmed de novo origins in 68.27%（185/271）of detected variants. Clinical phenotypic analysis demonstrated a significantly higher positive rate in isolated ID/GDD cases compared to those with comorbid autism spectrum disorder(ASD) or attention-deficit/hyperactivity disorder(ADHD)(P＜0.05). Conclusion：The combined analysis of WES and CNV significantly enhances molecular diagnostic yield for ID/GDD. High frequencies of MECP2 variants and 7q11.23 deletions s represent high-frequency findings in Chinese pediatric cohort. De novo variants constitute the primary genetic etiology in this cohort. These findings support the implementation of WES as a first-line clinical diagnostic tool for ID/GDD.