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["Table 6: The clinical information, prenatal diagnosis results and follow-up results of 15 cases with CNVs≥10M."]
["No","Age","Preg-\nweek","Indication","NIPT","Karyotype","CMA","Siginificance","Origin","Follow-up"]
[1,38,"26+0","Advanced age","Dup of 3q24-q29\n（146M-194M）","46,XX,der(8)t(3;8)(q24;p23)","3q24q29(144,804,358-197,851,444)x3,8p23.3p23.1(158,048-6,982,257)x1","Pathogenic","Unknown","Termination"]
[2,26,19,"Voluntary","Dup of 13q14.11-q21.32 \n(46-65M)","46,XN,dup(13)(q14q21)","13q14.11q21.32(43,450,607-66,726,903)x3","Pathogenic","Farther","Termination"]
[3,23,"17+2","Voluntary","Dup of 18p11.32-p11.21\n(1M-11M)","Normal","15q11.2(22,754,322-23,222,284)x1","Uncertain significance","Unknown","Unavailable"]
[4,24,"17+2","Voluntary","Dup of 4q24.3\n(119M-144M）","Normal","4p16.3p16.1(71,566-9,371,116)×1","Pathogenic","De novo","Termination"]
[5,30,"20+6","Voluntary","Del of Xq23-q28\n(110M-153M)","46,X,del(X)(q23)","Xp22.31(6,386,248-8,141,017)x3;Xq23q28(110,798,069-152,651,757)x1","Uncertain significance","Unknown","Normal female fetus"]
[6,31,"17+6","Voluntary","Dup of 19q13.2-q13.43\n(42M-57M)","Normal","11p14.1p13(27,473,981-33,896,715)x2 hmz","Uncertain significance","Unknown","Unavailable"]
[7,30,"17+6","High risk of serum screening","Del of 5p15.33-p13.3\n(1M-29M)","46,XN,del(5)(p14.2p15.3)","5p15.33p14.2(38,139-23,389,253)x1","Pathogenic","Unknown","Abnormal"]
[8,33,18,"High risk of serum screening","Del of5p15.33-p15.2\n(1M-15M)","46,XN,del(5)(p15.1)","5p15.33p15.1(113,576-16,275,896)x1","Pathogenic(cri-du-chat syndrome)","De novo","Termination"]
[9,22,"19+4","High risk of serum screening","Del of 5q14.3\n(80M-120M )","None","5q14.3q23.2(82,812,442-121,787,549)×1","Pathogenic","Unknown","Termination"]
[10,24,22,"Voluntary","Dup of 2q33.1-q37.3 \n(199M-241M)","46,XN,dup(2)(q33.1q37.1)","none","Pathogenic","Unknown","Termination"]
[11,25,"13+4","Voluntary","Del of11q12.1-q13.2\n（56M-67M）","Normal","16q23.1(77,909,692-78,568,430)x3","Pathogenic","Unknown","Normal"]
[12,38,16,"Voluntary","Dup of3q27.1-q29\n(183-196M)","None","4.8M del of5q35.2-5q35.3，","5q35 del syndrome  ","De novo","Fetal cardiac complex malformation"]
[13,24,19,"High risk of serum screening","Dup of 16q13.3-13.11(1-26M)，\ndup of 16q12.2-24.3(49-88M)","Normal","16p12.2(21,966,869-22,662,193)x1","Uncertain significance","Mother","Normal"]
[14,27,"19+4","High risk of serum screening","Dup of 10p15.3-p12.2\n(1M-23M)","46,XN,der(12)t(10;12)(p12.31;p13.31)","12p13.33p13.31(173,786-6,437,099)x1，10p15.3p12.31(100,047-20,255,943)x3","Pathogenic","Unknown","Termination"]
[15,24,"18+2","High risk of serum screening","Dup of 21q21.3-22.3\n(28M-46M)","46,XN,der(8)t(8;21)\n(p23.2;q21.3)","8p23.3p23.2(158,048-4,896,398)x1，21q21.3q22.3(27,985,829-48,093,361)x3","Pathogenic","Unknown","Termination"]

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