{"text_format":"3","workbook":"xls","n_sheets":3,"sheets":["Sheet1","Sheet2","Sheet3"],"read":"whole","date_system":"1900","formulas":"cached_only"}

{"sheet":"Sheet1","index":0,"n_rows":10,"n_cols":8,"rows_kept":10,"merged":[[0,0,0,7],[1,0,3,0],[1,1,3,1],[1,2,3,2],[1,3,3,3],[1,5,3,5],[1,6,3,6],[1,7,3,7]],"flags":["formulas_cached_only"]}
["Table 8: The clinical information, prenatal diagnosis results and follow-up results of six cases distal 22q11.2\n microdeletions and microduplications."]
["No","Age","Pregnant \nweek","22q Dup/del","Bp start; stop","Significance","Origin","Follow-up"]
[{"$nulls":4},"(NCBI37/hg19)"]
[]
[24,28,"16+6","Duplication","3p26.3(1,536,945-2,579,649)x3;\n22q11.21(18,844,632-21,462,353)x3","22q11.2 dup syndrome","Unknown","Normal"]
[29,25,"17+3","Duplication","22q11.21(18,648,855-21,800,471)x3","22q11.2 dup syndrome","Unknown","Normal"]
[30,31,20,"Duplication","22q11.21q11.23(21,059,669-24,629,406)x3","22q11.2 recurrent region\n (distal type I, D-E/F)","Unknown","Congenital heart malformation,\nventricular septal defect, aortic abnormalities"]
[34,31,"/","Loss of \nheterozygosity","22q12.1q12.2(28,317,927-30,826,759)x2 hmz","uncertain significance","Mother with 22q11.23\n(23,700,639-25,086,816)x3","Unavailable"]
[35,22,"26+2","Deletion","22q11.21(18,648,855-21,800,471)x1","DiGeorge syndrome","Unknown","Hoarseness, congenital heart disease"]
[37,32,"17+2","Duplication","22q11.21q11.23(21,464,120-23,650,987)x3","22q11.2 dup syndrome","Unknown","Normal"]

{"sheet":"Sheet2","index":1,"n_rows":0,"n_cols":0,"rows_kept":0,"flags":["formulas_cached_only"]}

{"sheet":"Sheet3","index":2,"n_rows":0,"n_cols":0,"rows_kept":0,"flags":["formulas_cached_only"]}